Label: RITE AID RYSHI SUNSCREEN FACE PRIMER SHEA BUTTER, ALOE, MINERAL OIL, AND VITAMIN E BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate, octocrylene lotion
- NDC Code(s): 11822-0049-1
- Packager: Rite Aid
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 15, 2023
If you are a consumer or patient please visit this version.
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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
aloe barbadensis leaf extract, Bis-vinyldimethicone/peg-10 dimethicone crosspolymer, butyloctyl salicylate, butyrospermum parkii (shea) butter, cetyl peg/ppg-10/1 dimethicone, citrus aurantium dulcis (orange) oil, dimethicone, dimethicone crosspolymer, dimethicone/vinyl dimethicone crosspolymer, disteardimonium hectorite, hexyl laurate, hydrated silica, isododecane, isohexadecane, lecithine, mineral oil, neopentyl glycol diethylhexanoate, phenoxyethanol, polyester-8, polyglyceryl-4 isostearate, polymethyl methacrylate, polymethylsilsequioxane, tocopherol
- Label
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INGREDIENTS AND APPEARANCE
RITE AID RYSHI SUNSCREEN FACE PRIMER SHEA BUTTER, ALOE, MINERAL OIL, AND VITAMIN E BROAD SPECTRUM SPF 30
avobenzone, homosalate, octisalate, octocrylene lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11822-0049 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 110 mg in 1 mL AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 30 mg in 1 mL OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 50 mg in 1 mL OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) ISOHEXADECANE (UNII: 918X1OUF1E) MINERAL OIL (UNII: T5L8T28FGP) ISODODECANE (UNII: A8289P68Y2) ORANGE OIL (UNII: AKN3KSD11B) DIMETHICONE/DIENE DIMETHICONE CROSSPOLYMER (UNII: RSA9I561OK) POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11) PHENOXYETHANOL (UNII: HIE492ZZ3T) SHEA BUTTER (UNII: K49155WL9Y) POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P) POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69) .ALPHA.-TOCOPHEROL, DL- (UNII: 7QWA1RIO01) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALOE VERA LEAF (UNII: ZY81Z83H0X) BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) HEXYL LAURATE (UNII: 4CG9F9W01Q) NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11822-0049-1 89 mL in 1 TUBE; Type 0: Not a Combination Product 12/20/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/20/2022 Labeler - Rite Aid (014578892)
