Label: RITE AID MINERAL SUNSCREEN BROAD SPECTRUM SPF 50- titanium dioxide, zinc oxide spray
- NDC Code(s): 11822-0058-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 20, 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 doctor if
- Keep out of reach of children.
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Directions
• spray liberally and spread evenly by hand 15 minutes before sun exposure
• hold can 4-6 inches away from skin top apply
• do not spray into face. Spray into hand and apply to face.
• use in a well ventilated areas
reapply:
• after 80 minutes of swimming or sweating
• immediately after towel drying
• at least every 2 hours• children under 6 months: 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, Isohexadecane, Isododecane, Caprylic/Capric Triglyceride, C12-15 Alkyl Benzoate, Neopentyl Glycol Diheptanoate, Shea Butter Ethyl Esters, Carthamus Tinctorius (Safflower) Seed Oil, C30-38 Olefin/Isopropyl Maleate/MA Copolymer, Butyloctyl Salicylate, Coco-Glucoside, Cetearyl Alcohol, Cetearyl Glucoside, Cetearyl Olivate, Sorbitan Olivate, Ethylhexylglycerin, Simmondsia Chinensis (Jojoba) Seed Oil, Sodium Hydroxide, Chlorphenesin, Xanthan Gum, Aloe Barbadensis Leaf Juice, Tocopherol, Glycerin, Sodium Gluconate, Citric Acid.
- Labels
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INGREDIENTS AND APPEARANCE
RITE AID MINERAL SUNSCREEN BROAD SPECTRUM SPF 50
titanium dioxide, zinc oxide sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0058 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 35 mg in 1 g ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 72.5 mg in 1 g Inactive Ingredients Ingredient Name Strength CHLORPHENESIN (UNII: I670DAL4SZ) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) ISODODECANE (UNII: A8289P68Y2) SORBITAN OLIVATE (UNII: MDL271E3GR) COCO GLUCOSIDE (UNII: ICS790225B) MAGNESIUM SULFATE HEPTAHYDRATE (UNII: SK47B8698T) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SAFFLOWER OIL (UNII: 65UEH262IS) ALOE VERA LEAF (UNII: ZY81Z83H0X) GLYCERIN (UNII: PDC6A3C0OX) XANTHAN GUM (UNII: TTV12P4NEE) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X) JOJOBA OIL (UNII: 724GKU717M) SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) WATER (UNII: 059QF0KO0R) ISOHEXADECANE (UNII: 918X1OUF1E) SODIUM HYDROXIDE (UNII: 55X04QC32I) CETYL ALCOHOL (UNII: 936JST6JCN) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ) CETEARYL GLUCOSIDE (UNII: 09FUA47KNA) CETEARYL OLIVATE (UNII: 58B69Q84JO) SODIUM GLUCONATE (UNII: R6Q3791S76) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0058-1 179 g in 1 CAN; Type 0: Not a Combination Product 01/10/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/10/2023 Labeler - Rite Aid (014578892)
