NDC 73036-004 Cryofreeze Roll-on Extra Strength
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 73036 - Omax Health, Inc
- 73036-004 - Cryofreeze Roll-on Extra Strength
Product Packages
NDC Code 73036-004-01
Package Description: 89 mL in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 73036-004?
What are the uses for Cryofreeze Roll-on Extra Strength?
Which are Cryofreeze Roll-on Extra Strength UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
Which are Cryofreeze Roll-on Extra Strength Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- 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)
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".