NDC 57329-010 Therafreeze
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 57329 - Astrum Pharma
- 57329-010 - Therafreeze
Product Packages
NDC Code 57329-010-01
Package Description: 473 mL in 1 TUBE
Product Details
What is NDC 57329-010?
What are the uses for Therafreeze?
Which are Therafreeze UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Therafreeze 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)
- WATER (UNII: 059QF0KO0R)
- ARCTIUM LAPPA ROOT (UNII: 597E9BI3Z3)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- CARBOMER HOMOPOLYMER TYPE C (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 4Q93RCW27E)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- WITCH HAZEL (UNII: 101I4J0U34)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- LAURETH-7 (UNII: Z95S6G8201)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Therafreeze?
- RxCUI: 1439987 - THERAFREEZE 6 % Topical Gel
- RxCUI: 1439987 - menthol 0.06 MG/MG Topical Gel [Therafreeze]
- RxCUI: 1439987 - Therafreeze 0.06 MG/MG Topical Gel
- RxCUI: 1439987 - Therafreeze 6 % Topical Gel
- RxCUI: 415976 - menthol 6 % Topical Gel
* Please review the disclaimer below.
[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".