Label: CRYO10 TOPICAL ANALGESIC- menthol gel
- NDC Code(s): 83549-000-01
- Packager: Element 26 LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 25, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Drug Facts
- Active Ingredient
- Uses
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Warnings
Avoid contact with eyes. For external use only.
Flammable: Keep away from fire or flame.
When using this product
• use only as directed • do not bandage tightly or use a heating pad • do not apply to wounds or damaged skin
- Directions
- Other Information
- Inactive Ingredients
- Package Labeling:
-
INGREDIENTS AND APPEARANCE
CRYO10 TOPICAL ANALGESIC
menthol gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:83549-000 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 100 mg in 1 mL Inactive Ingredients Ingredient Name Strength INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) EUCALYPTUS OIL (UNII: 2R04ONI662) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) GLYCERIN (UNII: PDC6A3C0OX) PEG-8 DIMETHICONE (UNII: GIA7T764OD) PENTYLENE GLYCOL (UNII: 50C1307PZG) PEPPERMINT OIL (UNII: AV092KU4JH) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:83549-000-01 88 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 05/26/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 05/26/2023 Labeler - Element 26 LLC (099970978)