Label: CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2% shampoo
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Contains inactivated NDC Code(s)
NDC Code(s): 72934-7058-6 - Packager: Sincerus Florida, LLC
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated May 16, 2019
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- Official Label (Printer Friendly)
- Sincerus Florida, LLC. Adverse reactions
- Directions for use
- Active, inactive
- NDC 72934- 7058-6 CLOBETASOL PROPIONATE USP 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE USP 2% . Shampoo 120 gm
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INGREDIENTS AND APPEARANCE
CLOBETASOL PROPIONATE 0.05% / LEVOCETIRIZINE DIHYDROCHLORIDE 2%
clobetasol propionate 0.05% / levocetirizine dihydrochloride 2% shampooProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-7058 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength 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 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-7058-6 120 g in 1 BOTTLE, PLASTIC; 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(72934-7058)
