VIRGO SOL NON TINTED MOUSSE- titanium dioxide, zinc oxide aerosol, foam

Virgo SOL Non Tinted Mousse by

Drug Labeling and Warnings

Virgo SOL Non Tinted Mousse by is a Otc medication manufactured, distributed, or labeled by ULTRAVIOLET SKINCARE LLC, Fragrance Manufacturing INC, Custom Analytics LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

PURPOSE

INDICATIONS & USAGE

WARNINGS

KEEP OUT OF REACH OF CHILDREN

DOSAGE & ADMINISTRATION

INACTIVE INGREDIENT

OTHER SAFETY INFORMATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

VIRGO SOL NON TINTED MOUSSE 
titanium dioxide, zinc oxide aerosol, foam

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85491-211
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	100 mg  in 1 g
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	30 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
CETEARETH-20 (UNII: YRC528SWUY)
CITRIC ACID (UNII: 2968PHW8QP)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
WATER (UNII: 059QF0KO0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
ISODODECANE (UNII: A8289P68Y2)
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
OCTYLDODECYL ERUCATE (UNII: D4N66T98C2)
C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
CELLULOSE GUM (UNII: K679OBS311)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
1,3,3,3-TETRAFLUOROPROPENE, (1E)- (UNII: 5I2481UOO8)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)
POLYSORBATE 80 (UNII: 6OZP39ZG8H)
TRIACONTANYL PVP (UNII: N0SS3Q238D)
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
GLYCERETH-26 (UNII: NNE56F2N14)
ISOHEXADECANE (UNII: 918X1OUF1E)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85491-211-04	100 g in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product	01/02/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	01/02/2023

Labeler - ULTRAVIOLET SKINCARE LLC (123592724)

Establishment
Name	Address	ID/FEI	Business Operations
Fragrance Manufacturing INC		793406000	manufacture(85491-211)

Establishment
Name	Address	ID/FEI	Business Operations
Custom Analytics LLC		144949372	analysis(85491-211)