CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2%- clobetasol propionate 0.05% / levocetirizine dihydrochloride 2% shampoo
Sincerus Florida, LLC

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2%

Sincerus Florida, LLC. Adverse reactions

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Directions for use

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Active, inactive

NDC 72934- 7058-6 CLOBETASOL PROPIONATE USP 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE USP 2% . Shampoo 120 gm

CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2%
clobetasol propionate 0.05% / levocetirizine dihydrochloride 2% shampoo

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC:72934-7058
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
CLOBETASOL PROPIONATE (UNII: 779619577M) (CLOBETASOL - UNII:ADN79D536H)	CLOBETASOL PROPIONATE	0.05 g in 100 g
LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA) (LEVOCETIRIZINE - UNII:6U5EA9RT2O)	LEVOCETIRIZINE DIHYDROCHLORIDE	2 g in 100 g

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:72934-7058-6	120 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	05/17/2019

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

Labeler - Sincerus Florida, LLC (080105003)

Name	Address	ID/FEI	Business Operations
Establishment
Sincerus Florida, LLC		080105003	manufacture(72934-7058)