Label: TRADER JOES ENRICH MOISTURIZING FACE BROAD SPECTRUM SPF 15- octinoxate, zinc oxide lotion
- NDC Code(s): 71270-252-11, 71270-252-14
- Packager: Trader Joe's Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 19, 2023
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- Official Label (Printer Friendly)
- Active ingredient
- Purpose
- Uses
- Warnings
- KEEP OUT OF REACH OF CHILDREN
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Directions
- Apply liberally on face and neck 15 minutes before sun exposure.
- Use a water resistant sunscreen if swimming or sweating.
- Reapply at least every 2 hours.
- Consult a doctor before use on children under six months of age.
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 15 value or higher along with 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.
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Inactive ingredients
ALLANTOIN, ASCORBIC ACID, CAPRYLYL GLYCOL, CETYL ALCOHOL, CHLORPHENESIN, CYCLOMETHICONE, CYCLOPENTASILOXANE, C13-14 ISOPARAFFIN, DIMETHICONE/VINYL DIMETHICONE CROSS POLYMER, DISODIUM EDTA, ETHYLHEXYLGLYCERIN, GLYCERIN, GLYCERYL STEARATE, HEXYLENE GLYCOL, ISOHEXADECANE, LAURETH-7 (COCONUT), PEG-100 STEARATE, PHENOXYETHANOL, POLYACRYLAMIDE, RETINYL PALMITATE (VITAMIN A), STEARYL ALCOHOL, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE, WATER.
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INGREDIENTS AND APPEARANCE
TRADER JOES ENRICH MOISTURIZING FACE BROAD SPECTRUM SPF 15
octinoxate, zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71270-252 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 ALLANTOIN (UNII: 344S277G0Z) ASCORBIC ACID (UNII: PQ6CK8PD0R) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CETYL ALCOHOL (UNII: 936JST6JCN) CHLORPHENESIN (UNII: I670DAL4SZ) CYCLOMETHICONE (UNII: NMQ347994Z) CYCLOMETHICONE 5 (UNII: 0THT5PCI0R) C13-14 ISOPARAFFIN (UNII: E4F12ROE70) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) EDETATE DISODIUM (UNII: 7FLD91C86K) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) GLYCERIN (UNII: PDC6A3C0OX) GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4) HEXYLENE GLYCOL (UNII: KEH0A3F75J) ISOHEXADECANE (UNII: 918X1OUF1E) LAURETH-7 (UNII: Z95S6G8201) PEG-100 STEARATE (UNII: YD01N1999R) PHENOXYETHANOL (UNII: HIE492ZZ3T) POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I) VITAMIN A PALMITATE (UNII: 1D1K0N0VVC) STEARYL ALCOHOL (UNII: 2KR89I4H1Y) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71270-252-11 29 mL in 1 TUBE; Type 0: Not a Combination Product 07/09/2019 2 NDC:71270-252-14 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/12/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/09/2019 Labeler - Trader Joe's Company (006226666)
