NDC | 69666-832-04 |
Set ID | 8483bbe9-6d27-482f-9055-a7af277ba069 |
Category | HUMAN OTC DRUG LABEL |
Packager | Genuine Drugs |
Generic Name | |
Product Class | Azole Antifungal |
Product Number | |
Application Number | PART333C |
- Drug Facts
- Active ingredient
- Purpose
- INDICATIONS & USAGE
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CAUTION:
CONTENTS UNDER PRESSURE. Do not expose to heat or open flame, or store at temperatures above 120 °F (50°C). Do not spray near naked flame or incandescent material. Do not spray toward face. If eye contact occurs, rinse eyes well with water. If irritation persists, contact a physician. Do not intentionally inhale vapor or spray mist. Avoid contamination of food. Store in a cool dry space. Protect from direct sunlight. Dispose of container properly. Do not puncture or incinerate even when empty.
USE ONLY AS DIRECTED: Intentional misuse by deliberately concentrating and inhaling the contents can be harmful and fatal. Help stop inhalant abuse, for more information, visit www.inhalant.org
- KEEP OUT OF REACH OF CHILDREN
- DIRECTIONS:
- INGREDIENTS:
- SPL UNCLASSIFIED SECTION
- Packaging
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INGREDIENTS AND APPEARANCE
BENGAMA - MICONAZOLE
miconazole nitrate aerosol, sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:69666-832 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MICONAZOLE NITRATE (UNII: VW4H1CYW1K) (MICONAZOLE - UNII:7NNO0D7S5M) MICONAZOLE NITRATE 20 mg in 1 g Inactive Ingredients Ingredient Name Strength PROPANE (UNII: T75W9911L6) ISOBUTANE (UNII: BXR49TP611) ALCOHOL (UNII: 3K9958V90M) TALC (UNII: 7SEV7J4R1U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:69666-832-04 1 in 1 BOX 11/01/2018 1 128 g in 1 CAN; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part333C 11/01/2018 Labeler - Genuine Drugs (079610378)