Label: RIVERSOL SPF 40 WEIGHTLESS BODY SUNSCREEN- weightless body sunscreen cream
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Contains inactivated NDC Code(s)
NDC Code(s): 72019-0004-1 - Packager: Riversol Skincare Solutions Inc
- Category: HUMAN OTC DRUG LABEL
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Drug Label Information
Updated December 30, 2020
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- ACTIVE INGREDIENT
- PURPOSE
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN
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WHEN USING
Apply liberally to face and body 15 minutes before sun exposure.Reapply after 40 minutes of swimming or sweatingimmediately after towel dryingat 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 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.
- PRECAUTIONS
- QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
RIVERSOL SPF 40 WEIGHTLESS BODY SUNSCREEN
weightless body sunscreen creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72019-0004 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 20.5 g in 100 g Inactive Ingredients Ingredient Name Strength AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG) METHYLCELLULOSE (100 CPS) (UNII: 4GFU244C4J) XANTHAN GUM (UNII: TTV12P4NEE) POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) PHYTATE SODIUM (UNII: 88496G1ERL) LONICERA CAPRIFOLIUM FLOWER (UNII: 5N1WD9784U) GINKGO BILOBA WHOLE (UNII: 660486U6OI) CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ) BAMBUSA ARUNDINACEA STEM (UNII: NRA4497HC5) POLYGLYCERYL-4 OLEATE (UNII: 15B05TY4GX) GLUCONOLACTONE (UNII: WQ29KQ9POT) HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O) SORBITAN MONOLAURATE (UNII: 6W9PS8B71J) JOJOBA OIL (UNII: 724GKU717M) LAURYL GLUCOSIDE (UNII: 76LN7P7UCU) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) POPULUS TREMULOIDES BARK (UNII: 5543O0CEID) TOCOPHEROL (UNII: R0ZB2556P8) OCTYLDODECYL LACTATE (UNII: 8JKW8M5W35) SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024) PHENOXYETHANOL (UNII: HIE492ZZ3T) SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL) SOYBEAN OIL (UNII: 241ATL177A) WATER (UNII: 059QF0KO0R) ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE (UNII: D2QHA03458) GLYCERIN (UNII: PDC6A3C0OX) DILAURYL CITRATE (UNII: 5OYS3G306B) ALOE VERA LEAF (UNII: ZY81Z83H0X) Product Characteristics Color white Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72019-0004-1 1 in 1 BOX 06/01/2020 1 140 g in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part352 06/01/2020 Labeler - Riversol Skincare Solutions Inc (203514773)