Label: CRYOFREEZE ROLL-ON REGULAR STRENGTH- menthol, unspecified form gel
-
Contains inactivated NDC Code(s)
NDC Code(s): 73036-003-01 - Packager: Omax Health, 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 March 18, 2022
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- When using this product
-
Inactive Ingredients
Aloe Barbadensis Leaf Extract, Arnica Montana Flower Extract, Boswellia Serrata Extract, Camphor, Industrial Hemp Extract, Carbomer, Chondroitin Sulfate, Ethylhexylglycerin, Glucosamine Sulfate, Glycerin, Ilex Paraguariensis Extract, Isopropyl Alcohol, Methyl Sulfonylmethane, Peppermint Oil, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Purified Water, Triethanolamine. No Parabens.
- Other Information
- PRINCIPAL DISPLAY PANEL - 89 mL Bottle Label
-
INGREDIENTS AND APPEARANCE
CRYOFREEZE ROLL-ON REGULAR STRENGTH
menthol, unspecified form gelProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:73036-003 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM 85 mg in 1 mL Inactive Ingredients Ingredient Name Strength ALOE VERA LEAF (UNII: ZY81Z83H0X) ARNICA MONTANA WHOLE (UNII: O80TY208ZW) INDIAN FRANKINCENSE (UNII: 4PW41QCO2M) CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) HEMP (UNII: TD1MUT01Q7) CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO) CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH) GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N) GLYCERIN (UNII: PDC6A3C0OX) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) ISOPROPYL ALCOHOL (UNII: ND2M416302) PHENOXYETHANOL (UNII: HIE492ZZ3T) ETHYLHEXYLGLYCERIN (UNII: 147D247K3P) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) PEPPERMINT OIL (UNII: AV092KU4JH) POLYSORBATE 20 (UNII: 7T1F30V5YH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:73036-003-01 89 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product 03/16/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph not final part348 03/16/2022 Labeler - Omax Health, Inc (965730778)