Label: LINIMENT- menthol gel
- NDC Code(s): 70489-1811-1, 70489-1811-2
- Packager: INNOVACYN INC.
- Category: OTC ANIMAL DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated December 5, 2023
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredient
- Description
- Dosage/Administration
- General Precautions
- Questions
- SPL UNCLASSIFIED SECTION
- Precautions
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Inactive Ingredient
Purified
Water, Ethyl Alcohol, Isocetyl Stearate, Glycerine,
Acrylates/C10-30 Alkyl Acrylate Crosspolymer,
Bisabolol, Heterotheca Inuloides Flower Extract
(and) Glycerin, Tocopherol (Vitamin E), Dimethicone,
Mentha Piperita (Peppermint) Oil, Helianthus Annuus
(Sunflower) Seed Oil, Phenoxyethanol, Triethanolamine,
Propylene Glycol / Menthol / Methyl Diisopropyl
Propionamide / Ethyl Menthane Carboxamide /
Methyl Lactate / Hydroxypropylcellulose / Acrylates,Copolymer, FD&C Blue #1
- Product label
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INGREDIENTS AND APPEARANCE
LINIMENT
menthol gelProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:70489-1811 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 7 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) ISOCETYL STEARATE (UNII: 3RJ7186O9W) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) LEVOMENOL (UNII: 24WE03BX2T) HETEROTHECA INULOIDES FLOWER (UNII: W9NZ9OZF68) TOCOPHEROL (UNII: R0ZB2556P8) DIMETHICONE (UNII: 92RU3N3Y1O) PEPPERMINT OIL (UNII: AV092KU4JH) SUNFLOWER SEED (UNII: R9N3379M4Z) SUNFLOWER OIL (UNII: 3W1JG795YI) PHENOXYETHANOL (UNII: HIE492ZZ3T) TROLAMINE (UNII: 9O3K93S3TK) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489) ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H) METHYL LACTATE, (-)- (UNII: 0379G9C44S) HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH) BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70489-1811-1 89 mL in 1 BOTTLE 2 NDC:70489-1811-2 473 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 08/01/2021 Labeler - INNOVACYN INC. (025217003)