us-fda-guidance-226f86e4f4f7197bbdb2adc9d5398cac•Policy On Maximum Timer Interval and Exposure Schedule For Sunlamp Products
Policy On Maximum Timer Interval and Exposure Schedule For Sunlamp Products
us-fda-guidance-226f86e4f4f7197bbdb2adc9d5398cacPolicy On Maximum Timer Interval and Exposure Schedule For Sunlamp ProductsGuidance
Administrative guidance, not enacted legislation. This captured publisher edition preserves the listed document and attachments; later developments are not independently consolidated.
- Docket Number:
- FDA-2020-D-0957
- Issued by:
- Guidance Issuing OfficeCenter for Devices and Radiological Health
The intended purposes of a sunlamp product timer are to provide for reliable control of exposures and to limit acute (and delayed) damage from unintentionally long exposures. However, the maximum timer setting should also allow for selection of exposure times needed to build up and maintain a tan. The maximum timer interval is in no way to be considered as a safe limit; all ultraviolet radiation is potentially hazardous.
Submit Comments
You can submit online or written comments on any guidance at any time (see 21 CFR 10.115(g)(5))
If unable to submit comments online, please mail written comments to:
Dockets Management
Food and Drug Administration
5630 Fishers Lane, Rm 1061
Rockville, MD 20852
All written comments should be identified with this document's docket number: FDA-2020-D-0957.
DEPARTMENT OF HEALTH & H U M A N SERVICES Public Health Service = . Food and Drug Adrnmistrat~on #16 2 1 (ge6 8 7 5 7 Georgia Avenue Sdver Sprmg MD 209 10 TO: A L L MANUFACTURERS, I M P O R T E R S AND P O T E N T I A L MANUFACTURERS O F SUNLAMP PRODUCTS. S U B J E C T : P O L I C Y ON MAXIMUM T I M E R I N T E R V A L AND EXPOSURE SCHEDULE F O R SUNLAMP PRODUCTS. BACKGROUND: The amended performance s t a n d a r d f o r sunlamp products ( 2 1 CFR 1040.29) was published i n t h e September 6, 1985 i s s u e of t h e Federal R e g i s t e r and w i l l become e f f e c t i v e September 8 , 1986. Any sunlamp product manufactured on o r a f t e r t h a t d a t e must comply with t h e amended standard. The t e n (10) minute maximum timer i n t e r v a l requirement was removed from t h e o r i g i n a l performance s t a n d a r d s i n c e t h e r e a r e newer sunlamp products on t h e market f o r which t e n (10) minutes is not a p p r o p r i a t e . The maximum timer i n t e r v a l now depends on t h e i n t e n s i t y and s p e c t r a l d i s t r i b u t i o n of u l t r a v i o l e t (W)r a d i a t i o n emission of each i n d i v i d u a l model of sunlamp product and must not exceed t h e maximum recommended exposure time provided on t h e r e q u i r e d product warning l a b e l . T h e r e f o r e , sunlamp product manufacturers must develop a n exposure schedule and e s t a b l i s h t h e maximum recommended exposure tlme (and t h e r e f o r e t h e maximum t i m e r i n t e r v a l ) based on t h e c h a r a c t e r i s t i c s o f t h e i r p a r t i c u l a r products. The intended purposes of a sunlamp product t i m e r a r e t o provide f o r r e l i a b l e c o n t r o l of exposures and t o l i m i t a c u t e (and delayed) damage from u n i n t e n t i o n a l l y long exposures. However, t h e maximum timer s e t t i n g ; should a l s o a l l o w f o r s e l e c t i o n o f exposure times needed t o b u i l d up and maintain a tan. The maxlmurn t i m e r i n t e r v a l i s i n no way t o be considered a s a s a f e l i m i t ; a l l u l t r a v i o l e t r a d i a t i o n is p o t e n t i a l l y hazardous. The s t a n d a r d r e q u i r e s t h e manufacturer t o provide a n exposure schedule i n t h e product warning l a b e l . The purpose o f t h e exposure schedule is t o a l l o w a person t o g r a d u a l l y build-up s k i n pigmentation and t o m a i n t a i n a t a n while c o n t r o l l i n g t h e r i s k of a c u t e i n j u r y and delayed a d v e r s e e f f e c t s . Since t h e W r a d i a t i o n dose t h a t causes a b a r e l y d i s c e r n i b l e pink c o l o r a t i o n (minimal erythema1 dose o r MED) is not t h e same f o r d i f f e r e n t s k i n t y p e s , t h e exposure schedule f o r f i r s t time u s e r s w i l l depend on t h e s k i n t y p e of t h e user. Furthermore, suberythemogenic doses of W r a d i a t i o n received at 24 hours i n t e r v a l s i n i t i a l l y l e a d t o lowering; of t h e erythema and t a n n i n g t h r e s h o l d s . Therefore, t h e exposure schedule and maximum recommended exposure t i m e should be c o n s t r a i n e d by t h e p o t e n t i a l f o r erythema a s w e l l as t h e q u a n t i t y of r a d i a t i o n necessary t o a c h i e v e and maintain a tan. POLICY : The Center f o r Devices and R a d i o l o g i c a l Health (CDRH) w i l l u s e t h e f o l l o w i n g c r i t e r i a t o e v a l u a t e t h e adequacy of t h e exposure schedule and t h e recommended maximum exposure t i m e (and t h e r e f o r e t h e maximum timer i n t e r v a l ) :
Page 2 1) The maximum recommended exposure time (and maximum timer interval) must not exceed a value which will result in an exposure of four (4) times the minimal erythema dose (MED) for untanned Type I1 skin (always burns, then tans slightly). This is based on the CDRH Erythema Action Spectrum [proposed action spectrum of Commission Internationale de L'Eclairage (CIE) modified by CDRHI. See Appendix A for the action spectrum and weighting factors and equations needed to derive it. The formula for determining the recommended maximum exposure . time,"T " in seconds is : e 2Te = 6 2 4 5 1 ~ ~ where Standard MED = 1565lM at 296nm CViRi vi = weighting factor Ri = irradiance in W/M2 2) The recommended maximum exposure time must not exceed a value which will result in an exposure of four (4) times the minimal melanogenic dose (MMD) for untanned Type I1 skin. This is based on the melanogenic action spectrum developed by Parrish et a1 (1982). See Appendix B for this action spectrum. The formula for " T ~ "in seconds determining the recommended maximum exposure time, is : 2 where standard MMD = 4 5 9 J / M at 296nm J~ = weighting factor tRi = irradiance in W/M2 3) The recommended exposure schedule should provide for exposures of no more than 0.75 MED three times the first week, gradually increasing the exposure the following weeks until maximum tanning has occurred (approximate,lyfour weeks total) and then provide for maintenance of a tan by biweekly or weekly exposures of up to four(4) MEDs or four(4) MMDs, whichever is less. CDRB believes that the above criteria balances the need to limit acute (and delayed) damages from unintentionally long exposure and the need to provide for single exposure durations adequate to achieve and maintain a tan. Walter E. Gundaker, Director Office of Compliance Center for De&es and Radiological Health Appendices
Appendix A (page 1) L n W E I G H T I N G F A C T O R S F O R E R Y T H E M A , V f W a v e l e n g t h ( n m ) t The equations . . . . describing the curve are:
Appendix A [DATA]GIELYTLE ERYTHEMA. Vi CIE ACTION SPECTRUM MODIFIED BY LYTLE (CDRH) NORMALIZED TO 1 AT READING 1 1 1 1 1 1 1 I 1 1 1 1 1 1 I 1 1 1 1 I 1 I I 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 .7691 5916 .4U
+ WAVELENGTH (nm) The MMD as function of wavelength has bean interpolated (using log MMD) fromrthe action spectrum tor melanogenesis of type 11 skin (~arrishet a1 1982)
Appendix B (page 2) TYPE I1 S K I N 1982
Vous vous demandez comment ce texte s’applique à votre situation ?
Consultation gratuite, sans engagement
Décrivez votre situation. Notre équipe vous recontactera par e-mail pour votre consultation.
Poursuivez vos recherches dans ChatGPT ou Claude
Connectez Omnilex pour rechercher dans le corpus juridique depuis votre assistant IA.