HYDROCORTISONE 2.5% / HYDROQUINONE 4% / TRETINOIN 0.025%, emulsion

HYDROCORTISONE 2.5% / HYDROQUINONE 4% / TRETINOIN 0.025%, by

Drug Labeling and Warnings

HYDROCORTISONE 2.5% / HYDROQUINONE 4% / TRETINOIN 0.025%, by is a Prescription medication manufactured, distributed, or labeled by Sincerus Florida, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Directions for use

Sincerus Florida, LLC. Adverse reactions

Active, inactive

NDC 72934- 6110-2 HYDROCORTISONE USP 2.5% / HYDROQUINONE USP 4% / TRETINOIN USP 0.025%. Emulsion 30 gm

INGREDIENTS AND APPEARANCE

HYDROCORTISONE 2.5% / HYDROQUINONE 4% / TRETINOIN 0.025%, 
hydrocortisone 2.5% / hydroquinone 4% / tretinoin 0.025%, emulsion

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 72934-6110
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HYDROQUINONE (UNII: XV74C1N1AE) (HYDROQUINONE - UNII:XV74C1N1AE)	HYDROQUINONE	4 g  in 100 g
HYDROCORTISONE (UNII: WI4X0X7BPJ) (HYDROCORTISONE - UNII:WI4X0X7BPJ)	HYDROCORTISONE	2.5 g  in 100 g

Product Characteristics
Color	yellow	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72934-6110-2	30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	05/17/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/17/2019

Labeler - Sincerus Florida, LLC (080105003)

Establishment
Name	Address	ID/FEI	Business Operations
Sincerus Florida, LLC		080105003	manufacture(72934-6110)