Label: DRS. PHARMACY SUNSCREEN SPF 50- sunscreen spf 50 lotion
- NDC Code(s): 80489-235-01, 80489-235-02
- Packager: OL PHARMA TECH LLC. (Drs. Pharmacy)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 1, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
- WARNINGS
- Do not use
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DOSAGE & ADMINISTRATION
- apply liberally 15 minutes before sun exposure.
- reapply after 80 minutes of swimming or sweating immediately after towel drying at least every 2 hours 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
- children under 6 months: Ask a doctor
- When using this product
- Stop use and ask a doctor
- Keep out of reach of children
- Inctive ingredients
- other information
- Questions
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
DRS. PHARMACY SUNSCREEN SPF 50
sunscreen spf 50 lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80489-235 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 5 g in 100 g HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 10 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 10 g in 100 g Inactive Ingredients Ingredient Name Strength GLYCERIN (UNII: PDC6A3C0OX) BENZYL ALCOHOL (UNII: LKG8494WBH) WATER (UNII: 059QF0KO0R) EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM) PEG-20 METHYL GLUCOSE SESQUISTEARATE (UNII: 0345752X7U) CYCLOMETHICONE (UNII: NMQ347994Z) CARBOMER COPOLYMER TYPE A (UNII: 71DD5V995L) XANTHAN GUM (UNII: TTV12P4NEE) ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T) SODIUM HYDRIDE (UNII: 23J3BHR95O) DOCOSANOL (UNII: 9G1OE216XY) PHENOXYETHANOL (UNII: HIE492ZZ3T) METHYL GLUCETH-20 (UNII: J3QD0LD11P) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D) ZINC OXIDE (UNII: SOI2LOH54Z) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80489-235-01 133 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2024 2 NDC:80489-235-02 118 g in 1 TUBE; Type 0: Not a Combination Product 01/01/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 01/01/2024 Labeler - OL PHARMA TECH LLC. (Drs. Pharmacy) (021170377) Registrant - OL PHARMA TECH LLC. (021170377) Establishment Name Address ID/FEI Business Operations OL PHARMA TECH LLC., (Drs. Pharmacy) 021170377 manufacture(80489-235)