NDC | 11822-3430-1 |
Set ID | 238c2336-dbff-4fbb-bcd7-2b3bc9339a11 |
Category | HUMAN OTC DRUG LABEL |
Packager | Rite Aid Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART352 |
- Active ingredients
- Uses
- Warnings
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Directions
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 sun, especially from 10 a.m. - 2 p.m.
- wear long-sleeved shirts, pants, hats, and sunglasses
- 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
- Other information
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Inactive ingredients
Water (Aqua), C12-15 Alkyl Benzoate, Caprylyl Methicone, Glcerin, Cetearyl Alcohol, Isohexadecane, Trimethylolpropane Triethylhexanoate, PEG-100 Stearate, Glyceryl Stearate, Butyloctyl Salicylate, Triethanolamine, Calcium Pantothenate, Bisabolol, Dicetyl Phosphate, Ceteth-10 Phosphate, Propylene Glycol, Butylene Glycol, Codium Tomentosum Extract, Caprylic/Capric Triglyceride, Sodium Acrylates Copolymer, Xanthan Gum, Phenoxyethanol, Methylparaben, Ethylparaben, Propylparaben, Isobtuylparaben, Butylparaben, Iron Oxides (CI 77491, CI 77492, CI 77499).
- Questions or comments?
- Label copy
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INGREDIENTS AND APPEARANCE
DAYLOGIC TINTED DAILY MOISTURIZER SPF 30
ensulizole, octinoxate, oxybenzone, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-3430 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 20 mg in 1 mL OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 75 mg in 1 mL OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 50 in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL) GLYCERIN (UNII: PDC6A3C0OX) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) ISOHEXADECANE (UNII: 918X1OUF1E) TRIMETHYLOLPROPANE TRIETHYLHEXANOATE (UNII: B952ZGW1IL) PEG-100 STEARATE (UNII: YD01N1999R) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) TROLAMINE (UNII: 9O3K93S3TK) DOCOSANOL (UNII: 9G1OE216XY) HYALURONATE SODIUM (UNII: YSE9PPT4TH) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1) CALCIUM PANTOTHENATE (UNII: 568ET80C3D) LEVOMENOL (UNII: 24WE03BX2T) DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N) CETETH-10 PHOSPHATE (UNII: 4E05O5N49G) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) CODIUM TOMENTOSUM (UNII: B8B45BRU87) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) SODIUM ACRYLATE (UNII: 7C98FKB43H) XANTHAN GUM (UNII: TTV12P4NEE) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYLPARABEN (UNII: A2I8C7HI9T) ETHYLPARABEN (UNII: 14255EXE39) PROPYLPARABEN (UNII: Z8IX2SC1OH) ISOBUTYLPARABEN (UNII: 0QQJ25X58G) BUTYLPARABEN (UNII: 3QPI1U3FV8) FERRIC OXIDE RED (UNII: 1K09F3G675) FERRIC OXIDE YELLOW (UNII: EX438O2MRT) FERROSOFERRIC OXIDE (UNII: XM0M87F357) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-3430-1 50 mL in 1 TUBE; Type 0: Not a Combination Product 08/13/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 08/13/2017 Labeler - Rite Aid Corporation (014578892) Registrant - Apollo Health and Beauty Care Inc. (201901209) Establishment Name Address ID/FEI Business Operations Apollo Health and Beauty Care Inc. 201901209 manufacture(11822-3430)