Label: ALL DAY MOISTURIZING SPF 15 EQB- octinoxate 6% zinc oxide 3% lotion
- NDC Code(s): 79903-210-06
- Packager: Walmart
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 17, 2023
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- Official Label (Printer Friendly)
- Active ingredients Purpose
- PURPOSE
- Uses
- Warnings For external use only
- Do not use on
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children. If swallowed,get medical help orcontact a Poison Control Center right away
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Directions:
• apply liberal 15 minutes before sun exposure• reapply at least every 2 hours •use a water resistant sunscreen if swimmingor sweating•children under 6 months of age: ask a doctor• Sun Protection Measures:Spending time in the sun increase your risk of skin cancer and early skin aging. To decrease this risk. regularly usea sunscreen wrtha Broad Spectrum SPF value of15 or higher and other suncrin protection measures including:
• limrt time in the sun, especial from 10a.m. -2 p.rn.•wear long-sleeve shorts , pants, hats and sunglasses -
Inactive Ingredients:
Water
Xanthan Gum
Disodium EDTA
Glycerin
Isohexadecane
Cyclopentasiloxane
Steareth-21
Stearyl Alcohol
Cetyl Alcohol
Steareth-2
Potassium Cetyl Phosphate
Octinoxate
Zinc Oxide, Triethoxycaprylylsilane
Tocopheryl Acetate
Behenyl Alcohol
Phenoxyethanol, Ethylhexylglycerin
Panthenol
Polyacrylamide, C13-14 Isoparaffin, Laureth-7
Sodium Polyacrylate, Dimethicone, Cyclopentasiloxane, Trideceth-6, PEG/PPG-18/18 Dimethicone
Aminomethyl Propanol
Aloe Barbadensis (Aloe Vera) Leaf Juice, Sodium Benzoate, Potassium Sorbate - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
ALL DAY MOISTURIZING SPF 15 EQB
octinoxate 6% zinc oxide 3% lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:79903-210 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 6 g in 100 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 3 g in 100 mL Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) ISOHEXADECANE (UNII: 918X1OUF1E) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) STEARETH-2 (UNII: V56DFE46J5) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT) SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L) DIMETHICONE (UNII: 92RU3N3Y1O) TRIDECETH-6 (UNII: 3T5PCR2H0C) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) STEARETH-21 (UNII: 53J3F32P58) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) DOCOSANOL (UNII: 9G1OE216XY) CETYL ALCOHOL (UNII: 936JST6JCN) POLYACRYLAMIDE (1500 MW) (UNII: 5D6TC4BRWV) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) LAURETH-7 (UNII: Z95S6G8201) ALOE (UNII: V5VD430YW9) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) XANTHAN GUM (UNII: TTV12P4NEE) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PANTHENOL (UNII: WV9CM0O67Z) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:79903-210-06 1 in 1 CARTON 10/17/2023 1 177 mL in 1 CONTAINER; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M006 08/09/2023 Labeler - Walmart (051957769) Registrant - Bridgeview Investments, LLC (035014854) Establishment Name Address ID/FEI Business Operations Dimensional Merchandising Inc 076693183 manufacture(79903-210)
