Label: ILLUMINATING DAILY MOISTURIZER SPF 15- avobenzone, octinoxate, octisalate lotion
-
Contains inactivated NDC Code(s)
NDC Code(s): 59779-601-05 - Packager: CVS Pharmacy
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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 April 16, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Use(s)
- Warnings
-
Directions
- apply liberally 15 minutes before sun exposure.
- reapply at least every 2 hours.
- use a water resistant sunscreen if swimming or sweating.
- 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 (Aqua), C12-15 Alkyl Benzoate, Diethylhexyl 2,6 Naphthalate, Cetearyl Alcohol, Dimethicone, Glycine Soja (Soybean) Seed Extract, Glyceirn, BIS-Phenylpropyl Dimethicone, Arachidyl Alcohol, Phenoxyethanol, Cetearyl Glucoside, Panthenol, Benzyl Alcohol, Ethylene/Acrylic Acid Copolymer, Behenyl Alcohol, Steareth-2, Fragrance (Parfum), Steareth-12, Polyacrylamide, Nylon 10-10, Arachidyl Glucoside, Disodium EDTA, C13-14 Isoparaffin, Ethylhexylglycerin, Laureth-7, Benzalkonium Chloride, Sodium Hydroxide, Iodopropynyl Butylcarbamate, BHT, Titanium Dioxide (CI 77891), Mica.
- Label Copy
-
INGREDIENTS AND APPEARANCE
ILLUMINATING DAILY MOISTURIZER SPF 15
avobenzone, octinoxate, octisalate lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59779-601 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 20 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) DIMETHICONE (UNII: 92RU3N3Y1O) SOYBEAN (UNII: L7HT8F1ZOD) GLYCERIN (UNII: PDC6A3C0OX) BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT) ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU) PHENOXYETHANOL (UNII: HIE492ZZ3T) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) PANTHENOL (UNII: WV9CM0O67Z) BENZYL ALCOHOL (UNII: LKG8494WBH) ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I) DOCOSANOL (UNII: 9G1OE216XY) STEARETH-2 (UNII: V56DFE46J5) STEARETH-21 (UNII: 53J3F32P58) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) NYLON-12 (UNII: 446U8J075B) ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ) EDETATE DISODIUM (UNII: 7FLD91C86K) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) LAURETH-7 (UNII: Z95S6G8201) BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) SODIUM HYDROXIDE (UNII: 55X04QC32I) IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) MICA (UNII: V8A1AW0880) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59779-601-05 118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/13/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 04/13/2018 Labeler - CVS Pharmacy (062312574) Registrant - Apollo Health and Beauty Care Inc. (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care Inc. 201901209 manufacture(59779-601)