Label: RITE AID MINERAL SENSITIVE SKIN ZINC OXIDE SUNSCREEN FOR FACE SPF 50- zinc oxide lotion
- NDC Code(s): 11822-0052-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
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- Official Label (Printer Friendly)
- Active ingredients
- Purpose
- Uses
- Warnings
- Do not use
- When using this product
- 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:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours
• children under 6 months of age: Ask a doctor
- 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 the sun, especially from 10 a.m. - 2 p.m.
• wear long-sleeved shirts, pants, hats, and sunglasses
- Other information
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Inactive ingredients
water, C12-15 alkyl benzoate, caprylic/capric triglyceride, styrene/acrylates copolymer, cetyl PEG/PPG-10/1 dimethicone, octyldodecyl citrate crosspolymer, phenyl trimethicone, dimethicone, polyhydroxystearic acid, glycerin, ethyl methicone, cetyl dimethicone, silica, colloidal oatmeal, chrysanthemum parthenium (feverfew) flower/leaf/stem juice, glyceryl behenate, phenethyl alcohol, caprylyl glycol, bis-divinyl dimethicone PEG-10 dimethicone crosspolymer, sodium chloride, phenoxyethanol, chlorphenesin
- Label
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INGREDIENTS AND APPEARANCE
RITE AID MINERAL SENSITIVE SKIN ZINC OXIDE SUNSCREEN FOR FACE SPF 50
zinc oxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0052 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION 216 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) OCTYLDODECYL CITRATE CROSSPOLYMER (UNII: X323T6QO4M) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) DIMETHICONE (UNII: 92RU3N3Y1O) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) GLYCERIN (UNII: PDC6A3C0OX) ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H) CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) OATMEAL (UNII: 8PI54V663Y) GLYCERYL MONOBEHENATE (UNII: A626UU0W2A) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SODIUM CHLORIDE (UNII: 451W47IQ8X) PHENOXYETHANOL (UNII: HIE492ZZ3T) CHLORPHENESIN (UNII: I670DAL4SZ) TANACETUM PARTHENIUM FLOWER (UNII: 7TVV9D7I89) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0052-1 89 mL in 1 TUBE; Type 0: Not a Combination Product 12/21/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/21/2022 Labeler - Rite Aid (014578892)
