RIVERSOL SPF 40 WEIGHTLESS BODY SUNSCREEN- weightless body sunscreen cream

Riversol SPF 40 Weightless Body Sunscreen by

Drug Labeling and Warnings

Riversol SPF 40 Weightless Body Sunscreen by is a Otc medication manufactured, distributed, or labeled by Riversol Skincare Solutions Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Oxide 20.5%

PURPOSE

Sunscreen

WARNINGS

For external use only.Do not use on damaged or broken skin.When using this product, keep out of eyes. Rinse with water to remove.Stop use and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

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

Protect the product in this container from excessive heat and direct sunstore at room temperature 59-86°F (15-30°C)May stain some fabrics.

QUESTIONS

Call toll free 1-866-774-8377 or visit www.riversol.com

PRINCIPAL DISPLAY PANEL

RIversol

Weightless Body Sunscreen

Broad spectrum, hypoallergenic lotion

SPF 40 UVA / UVB protection

Rubs in Clear, Non-whitening

Fast absorbing, Fragrance-Free

Reef-Safe, Mineral Sun Filter (Zinc Oxide)

Water / Sweat Resistant (40 MIN)

nt wt. 140g (4.9 oz)

INGREDIENTS AND APPEARANCE

RIVERSOL SPF 40 WEIGHTLESS BODY SUNSCREEN 
weightless body sunscreen cream

Product 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)