NDC 53113-363 Frozen Ice Fast Pain Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53113 - Gadal Laboratories, Inc
- 53113-363 - Frozen Ice Fast Pain Relief
Product Packages
NDC Code 53113-363-03
Package Description: 89 mL in 1 APPLICATOR
Product Details
What is NDC 53113-363?
What are the uses for Frozen Ice Fast Pain Relief?
Which are Frozen Ice Fast Pain Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941) (Active Moiety)
Which are Frozen Ice Fast Pain Relief 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:
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- TROLAMINE (UNII: 9O3K93S3TK)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Frozen Ice Fast Pain Relief?
- RxCUI: 416207 - camphor 0.2 % / menthol 3.5 % Topical Gel
- RxCUI: 416207 - camphor 0.002 MG/MG / menthol 0.035 MG/MG Topical Gel
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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".