Label: DAYLOGIC TINTED DAILY MOISTURIZER SPF 30- ensulizole, octinoxate, oxybenzone, zinc oxide lotion
-
Contains inactivated NDC Code(s)
NDC Code(s): 11822-3430-1 - Packager: Rite Aid Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not 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 August 14, 2017
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients
- Uses
- Warnings
-
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
-
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
-
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)
