NDC 71473-067 Max-relief With Boswellia And Aloe Vera
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71473 - Usconsultancy For Applied Research
- 71473-067 - Max-relief With Boswellia And Aloe Vera
Product Packages
NDC Code 71473-067-02
Package Description: 1 TUBE in 1 CARTON / 56.7 g in 1 TUBE
Product Details
What is NDC 71473-067?
What are the uses for Max-relief With Boswellia And Aloe Vera?
Which are Max-relief With Boswellia And Aloe Vera 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)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Max-relief With Boswellia And Aloe Vera 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)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- EDETATE SODIUM (UNII: MP1J8420LU)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Max-relief With Boswellia And Aloe Vera?
- RxCUI: 1927954 - camphor 6 % / menthol 7 % Topical Gel
- RxCUI: 1927954 - camphor 0.06 MG/MG / menthol 0.07 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".