NDC 70316-360 Sno Swedish Arctic Gel Recovery
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 70316-360?
What are the uses for Sno Swedish Arctic Gel Recovery?
Which are Sno Swedish Arctic Gel Recovery 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 Sno Swedish Arctic Gel Recovery 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:
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CALENDULA OFFICINALIS FLOWERING TOP (UNII: 18E7415PXQ)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOSTEARYL ISOSTEARATE (UNII: IV0Z586Z4Y)
- RUSCOGENIN (UNII: BXI92R2VUJ)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
What is the NDC to RxNorm Crosswalk for Sno Swedish Arctic Gel Recovery?
- RxCUI: 1730427 - menthol 2.25 % Topical Gel
- RxCUI: 1730427 - menthol 0.0225 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".