SUNSOVLE MD VOLUMIZE AND RESTORE- zinc oxide lotion

Sunsovle MD Volumize and Restore by

Drug Labeling and Warnings

Sunsovle MD Volumize and Restore by is a Otc medication manufactured, distributed, or labeled by Sunsolve MD Inc, Nanophase Technologies Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

Sunsovle MD Volumize and Restore

INGREDIENTS AND APPEARANCE

SUNSOVLE MD VOLUMIZE AND RESTORE 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84878-823
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	110 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ETHYL STEARATE (UNII: C64RTC734W)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
SQUALANE (UNII: GW89575KF9)
ISODODECANE (UNII: A8289P68Y2)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
TOCOPHEROL (UNII: R0ZB2556P8)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
COCO-CAPRYLATE (UNII: 4828G836N6)
ETHYL OLEATE (UNII: Z2Z439864Y)
RUTIN (UNII: 5G06TVY3R7)
PENTAERYTHRITYL TETRA-DI-T-BUTYL HYDROXYHYDROCINNAMATE (UNII: 255PIF62MS)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
LIMNANTHES ALBA (MEADOWFOAM) SEED OIL (UNII: 412ZHA4T4Y)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
BUTYROSPERMUM PARKII (SHEA) BUTTER UNSAPONIFIABLES (UNII: 0C9AC7D6XU)
ETHYL PALMITATE (UNII: IRD3M534ZM)
ISOHEXADECANE (UNII: 918X1OUF1E)
C13-15 ALKANE (UNII: 114P5I43UJ)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84878-823-02	1 in 1 CARTON	11/05/2024
1	NDC: 84878-823-01	50 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	11/05/2024

Labeler - Sunsolve MD Inc (119376976)

Registrant - Nanophase Technologies Corporation (623502044)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		050383046	api manufacture(84878-823)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		118812921	manufacture(84878-823) , pack(84878-823)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		623502044	manufacture(84878-823) , api manufacture(84878-823)