Label: SKINPHARMACY ADVANCED ANTI-AGING THERAPY RETINOL DAY MOISTURIZER SPF 30- homosalate, octisalate, avobenzone, octocrylene, oxybenzone liquid
- NDC Code(s): 68634-056-01
- Packager: AMCOL Health & Beauty Solutions, Inc. DBA
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 7, 2016
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- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredients
- Purpose
-
Uses
- Helps prevent sunburn
- If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging cause by the sun.
- Warnings
-
Directions
- Apply liberally 15 minutes before sun exposure
- Use a water resistant sunscreen if swimming or sweating
- Reapply at least every 2 hours
- Children under 6 months: Ask a doctor
-
Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
- limit time in the sun, especially from 10 a.m.-2 p.m.
- wear long-sleeved shirts, pants, hats and sunglasses
- Other information
-
Inactive ingredients
Water, C12-15 Alkyl Benzoate, Butylene Glycol, Glycerin, Potassium Cetyl Phosphate, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Arachidyl Alcohol, Dimethicone, Glyceryl Myristate, PEG-100 Stearate, Sodium Hyaluronate, Retinol, Picea Abies Wood Extract, Ethylhexylglycerin, Tocopherol Acetate, Dipotassium Glycyrrhizate, Arachidyl Glucoside, Bentonite, Allylmethacrylates Crosspolymer, Acrylates/C10-30 Alkylacrylate Crosspolymer, Behenyl Alcohol, Sodium Hydroxide, Disodium EDTA, BHT, Erythorbic Acid, Polysorbate 20, Chlorphenesin, Titanium Dioxide, Ascorbic Acid, Propyl Gallate, Phenoxyethanol.
Microsponge® and Polargel® are registered trademarks of AMCOL International Corp.
Distributed by: CVS Pharmacy, Inc.
One CVS Drive, Woonsocket, RI 02895
© 2014 CVS/pharmacy
CVS.com® 1-800-SHOP CVS
Made in the U.S.A. of U.S. and imported components
V-31490
CVS® Quality
Money Back Guarantee
#979865
M050769CP
FP114
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PRINCIPAL DISPLAY PANEL
Principal Display Panel - Skin+Pharmacy Advanced Anti-Aging Therapy Carton Label
DAY
SKIN+PHARMACY
ADVANCED
ANTI-AGING THERAPYRETINOL DAY MOISTURIZER
with Microsponge®
& Polargel® Technologies0.15% Retinol & SPF 30
Broad Spectrum Screen
- Retinol is clinically proven
to reduce the appearance
of fine lines & wrinkles - protects skin from harmful
UVA & UVB rays - fragrance- &
oil-free formula
exclusively at
CVS/pharmacy
DERMATOLOGIST TESTED
Actual Size Product on Side Panel
1 FL OZ (30 mL)
- Retinol is clinically proven
-
PRINCIPAL DISPLAY PANEL
Principal Display Panel - Skin+Pharmacy Advanced Anti-Aging Therapy Label
SKIN+PHARMACY
ADVANCED
ANTI-AGING THERAPYRETINOL DAY MOISTURIZER
with Microsponge®
& Polargel® Technologies0.15% Retinol & SPF 30
Broad Spectrum Screen- Retinol is clinically proven
to reduce the appearance
of fine lines & wrinkles - protects skin from harmful
UVA & UVB rays - fragrance- &
oil-free formula
exclusively at
CVS/pharmacy
DERMATOLOGIST TESTED
1 FL OZ (30 mL)
- Retinol is clinically proven
-
INGREDIENTS AND APPEARANCE
SKINPHARMACY ADVANCED ANTI-AGING THERAPY RETINOL DAY MOISTURIZER SPF 30
homosalate, octisalate, avobenzone, octocrylene, oxybenzone liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:68634-056 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength homosalate (UNII: V06SV4M95S) (homosalate - UNII:V06SV4M95S) homosalate 100 mg in 1 mL octisalate (UNII: 4X49Y0596W) (octisalate - UNII:4X49Y0596W) octisalate 50 mg in 1 mL avobenzone (UNII: G63QQF2NOX) (avobenzone - UNII:G63QQF2NOX) avobenzone 20 mg in 1 mL octocrylene (UNII: 5A68WGF6WM) (octocrylene - UNII:5A68WGF6WM) octocrylene 15 mg in 1 mL oxybenzone (UNII: 95OOS7VE0Y) (oxybenzone - UNII:95OOS7VE0Y) oxybenzone 40 mg in 1 mL Inactive Ingredients Ingredient Name Strength water (UNII: 059QF0KO0R) butylene glycol (UNII: 3XUS85K0RA) polyethylene glycol 400 (UNII: B697894SGQ) high density polyethylene (UNII: UG00KM4WR7) dimethicone (UNII: 92RU3N3Y1O) tetrapeptide-21 (UNII: 179JUC43HU) hexyldecanol (UNII: 151Z7P1317) picea abies wood (UNII: 72GZ8K8996) rapeseed sterol (UNII: B46B6DD20U) aloe vera leaf (UNII: ZY81Z83H0X) sodium ascorbyl phosphate (UNII: 836SJG51DR) cetylhydroxyproline palmitamide (UNII: 74ONU0S62G) wheat germ (UNII: YR3G369F5A) glycerin (UNII: PDC6A3C0OX) levomenol (UNII: 24WE03BX2T) tocopherol (UNII: R0ZB2556P8) vitamin a palmitate (UNII: 1D1K0N0VVC) .alpha.-tocopherol acetate, DL- (UNII: WR1WPI7EW8) sodium polyacrylate (8000 mw) (UNII: 285CYO341L) carbomer copolymer type A (UNII: 71DD5V995L) lauryl glucoside (UNII: 76LN7P7UCU) titanium dioxide (UNII: 15FIX9V2JP) bentonite (UNII: A3N5ZCN45C) stearic acid (UNII: 4ELV7Z65AP) edetate disodium (UNII: 7FLD91C86K) ethylhexylglycerin (UNII: 147D247K3P) phenoxyethanol (UNII: HIE492ZZ3T) chlorphenesin (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:68634-056-01 1 in 1 CARTON 10/01/2014 1 30 mL in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 10/01/2014 Labeler - AMCOL Health & Beauty Solutions, Inc. DBA (872684803) Establishment Name Address ID/FEI Business Operations AMCOL Health & Beauty Solutions, Inc. DBA 872684803 MANUFACTURE(68634-056) , PACK(68634-056) , LABEL(68634-056) , ANALYSIS(68634-056)
