Label: NUMOTIZINE- menthol ointment
- NDC Code(s): 10546-100-08, 10546-100-35
- Packager: Hobart Laboratories, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 20, 2023
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- Official Label (Printer Friendly)
- NUMOTIZINE OINTMENT
- Active Ingredients
- Purpose
- Inactive ingredients
- Directions
- Uses
- Stop use and ask a doctor if
- Keep out of the reach of children
- Warnings:
- Representative Labeling For - Numotizine Ointment 3.5oz/99g (10546-100-35) | Numotizine Ointment 8oz/228g (10546-100-08)
- Package Labeling:
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INGREDIENTS AND APPEARANCE
NUMOTIZINE
menthol ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10546-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.25 g in 100 g Inactive Ingredients Ingredient Name Strength KAOLIN (UNII: 24H4NWX5CO) GUAIACOL (UNII: 6JKA7MAH9C) CREOSOL (UNII: W9GW1KZG6N) METHYL SALICYLATE (UNII: LAV5U5022Y) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) Product Characteristics Color pink Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10546-100-35 99 g in 1 JAR; Type 0: Not a Combination Product 11/30/2011 2 NDC:10546-100-08 228 g in 1 JAR; Type 0: Not a Combination Product 11/30/2011 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 11/30/2011 Labeler - Hobart Laboratories, Inc. (005111786) Registrant - Hobart Laboratories, Inc. (005111786) Establishment Name Address ID/FEI Business Operations Hobart Laboratories, Inc. 005111786 manufacture(10546-100)