Label: ECONAZOLE NITRATE 1% / NIACINAMIDE 4% cream
- Category: HUMAN PRESCRIPTION DRUG LABEL
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.
Updated May 20, 2019
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- Directions for use
- Sincerus Florida, LLC. Adverse reactions
- Active, inactive
- NDC 72934- 2073-2 ECONAZOLE NITRATE USP 1% / NIACINAMIDE USP 4%. Cream 30 gm
INGREDIENTS AND APPEARANCE
ECONAZOLE NITRATE 1% / NIACINAMIDE 4%
econazole nitrate 1% / niacinamide 4% cream
Product Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:72934-2073 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ECONAZOLE NITRATE (UNII: H438WYN10E) (ECONAZOLE - UNII:6Z1Y2V4A7M) ECONAZOLE NITRATE 1 g in 100 g NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE 4 g in 100 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72934-2073-2 30 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product 05/20/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 05/20/2019 Labeler - Sincerus Florida, LLC (080105003) Establishment Name Address ID/FEI Business Operations Sincerus Florida, LLC 080105003 manufacture(72934-2073)