Label: EPOCH- alcohol gel
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Contains inactivated NDC Code(s)
NDC Code(s): 62839-1083-3, 62839-1083-4 - Packager: NSE Products, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph not final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated January 12, 2022
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- Active Ingredient
- Purpose
- Usage
- Warnings
- Directions
- Inactive Ingredients:
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- SPL UNCLASSIFIED SECTION
- PRINCIPAL DISPLAY PANEL - 100 ml Bottle Label
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INGREDIENTS AND APPEARANCE
EPOCH
alcohol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:62839-1083 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Alcohol (UNII: 3K9958V90M) (Alcohol - UNII:3K9958V90M) Alcohol 61.9937 mL in 100 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) LAVENDER OIL (UNII: ZBP1YXW0H8) LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y) POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F) AMINOMETHYLPROPANOL (UNII: LU49E6626Q) CHLORPHENESIN (UNII: I670DAL4SZ) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:62839-1083-3 100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/01/2009 2 NDC:62839-1083-4 30 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/27/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH NOT FINAL part333E 06/01/2009 Labeler - NSE Products, Inc. (803486393)