Label: COMPLETE BEAUTY- octinoxate, zinc oxide lotion
- NDC Code(s): 41250-955-30
- Packager: Meijer
- 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 July 26, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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Claims
- LIGHT, NON-GREASY FORMULA
- DERMATOLOGIST
- WON'T CLOG PORES
- FRAGRANCE FREE
When used as directed, Meijer Beauty Lotion helps provide your skin with broad spectrum protecton against premature skin damage from both UVA and UVB rays to help your skin stay younger looking.
ALL DAY MOISTURIZER- This formula with antoxidant vitamin E plus aloe helps promote and maintain healthy-looking skin
- Active ingredient
- Purpose
- Uses
- Warnings
- Do Not Use
- Stop use and ask a doctor if
- Keep out of reach of children
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Directions
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- 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 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
- children under 6 months of age: ask a doctor
- Other information
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Inactive ingredients
water, glycerin, isohexadecane, sodium acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, laureth-7, PEG/PPG-20/20 dimethicone, steareth-21, stearyl alcohol, Gossypium herbaceum (cotton) seed oil, behenyl alcohol, tocopheryl acetate, cetyl alcohol, steareth-2, disodium EDTA, Aloe barbadensis leaf extract, oleth-3 phosphate, benzyl alcohol, chlorphenesin
- Disclaimer
- Adverse Reactions
- principl display panel
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INGREDIENTS AND APPEARANCE
COMPLETE BEAUTY
octinoxate, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-955 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 60 mg in 1 mL ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) GLYCERIN (UNII: PDC6A3C0OX) ISOHEXADECANE (UNII: 918X1OUF1E) SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX) POLYSORBATE 80 (UNII: 6OZP39ZG8H) LAURETH-7 (UNII: Z95S6G8201) PEG/PPG-20/20 DIMETHICONE (UNII: BA94B7CK8K) STEARETH-21 (UNII: 53J3F32P58) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) LEVANT COTTONSEED OIL (UNII: N5CFT140R8) DOCOSANOL (UNII: 9G1OE216XY) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) CETYL ALCOHOL (UNII: 936JST6JCN) STEARETH-2 (UNII: V56DFE46J5) EDETATE DISODIUM (UNII: 7FLD91C86K) ALOE VERA LEAF (UNII: ZY81Z83H0X) OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL) BENZYL ALCOHOL (UNII: LKG8494WBH) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-955-30 1 in 1 CARTON 05/05/2019 1 177 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part352 05/05/2019 Labeler - Meijer (006959555) Registrant - Vi-Jon, LLC (790752542) Establishment Name Address ID/FEI Business Operations Vi-Jon, LCC 790752542 manufacture(41250-955) Establishment Name Address ID/FEI Business Operations Vi-Jon, LCC 088520668 manufacture(41250-955)
