GUISE TINTED DROPS- zinc oxide lotion

Guise Tinted Drops by

Drug Labeling and Warnings

Guise Tinted Drops by is a Otc medication manufactured, distributed, or labeled by Donis Men LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

Guise Tinted Drops

INGREDIENTS AND APPEARANCE

GUISE TINTED DROPS 
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83827-1208
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
LAURYL PEG-8 DIMETHICONE (300 CPS) (UNII: ELL2U7K8T8)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
WATER (UNII: 059QF0KO0R)
POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)
DIMETHICONE (UNII: 92RU3N3Y1O)
NIACINAMIDE (UNII: 25X51I8RD4)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)
TRILAURETH-4 PHOSPHATE (UNII: M96W2OLL2V)
DIMETHICONOL/PROPYLSILSESQUIOXANE/SILICATE CROSSPOLYMER (450000000 MW) (UNII: 9KB5R958PB)
PROPANEDIOL (UNII: 5965N8W85T)
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
FERRIC OXIDE RED (UNII: 1K09F3G675)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
.ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
ISODODECANE (UNII: A8289P68Y2)
ALLANTOIN (UNII: 344S277G0Z)

Product Characteristics
Color	pink	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83827-1208-2	1 in 1 CARTON	02/11/2025
1	NDC: 83827-1208-1	30 mL 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 Drug	M020	02/11/2025

Labeler - Donis Men LLC (127109241)