SUNSOLVE MD BALANCE AND CLEAR- zinc oxide lotion

Sunsolve MD Balance and Clear by

Drug Labeling and Warnings

Sunsolve MD Balance and Clear 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]

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

Sunsolve MD Balance and Clear

INGREDIENTS AND APPEARANCE

SUNSOLVE MD BALANCE AND CLEAR 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84878-997
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	132 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CAMELLIA SINENSIS LEAF OIL (UNII: VC855RRT77)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
EUTERPE OLERACEA FRUIT OIL (UNII: Z0W6766A2W)
CARAPA GUIANENSIS SEED OIL (UNII: Y82418EH2I)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
COPAIFERA OFFICINALIS (BALSAM COPAIBA) RESIN (UNII: 1VH544O5AT)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
JOJOBA OIL (UNII: 724GKU717M)
ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)
TRIDECYL SALICYLATE (UNII: AZQ08K38Z1)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
COCO-CAPRYLATE (UNII: 4828G836N6)
NYLON-12 (UNII: 446U8J075B)
PHENYLPROPANOL (UNII: 0F897O3O4M)
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
METHYLPROPANEDIOL (UNII: N8F53B3R4R)
POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)
ALLANTOIN (UNII: 344S277G0Z)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
NIACINAMIDE (UNII: 25X51I8RD4)
PROPANEDIOL (UNII: 5965N8W85T)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
POLYGLYCERYL-4 DIISOSTEARATE/POLYHYDROXYSTEARATE/SEBACATE (UNII: 687U3PEB2Y)
POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
STEARALKONIUM HECTORITE (UNII: OLX698AH5P)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84878-997-02	1 in 1 CARTON	11/06/2024
1	NDC: 84878-997-01	48 mL in 1 BOTTLE, PUMP; 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	11/06/2024

Labeler - Sunsolve MD Inc (119376976)

Registrant - Nanophase Technologies Corporation (623502044)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		050383046	api manufacture(84878-997)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		118812921	pack(84878-997) , manufacture(84878-997)

Establishment
Name	Address	ID/FEI	Business Operations
Nanophase Technologies Corporation		623502044	api manufacture(84878-997) , manufacture(84878-997)