NDC 70759-0012 Aquacool Multi 500
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 70759 - Pharmanuco
- 70759-0012 - Aquacool Multi 500
Product Packages
NDC Code 70759-0012-1
Package Description: 500 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 70759-0012?
What are the uses for Aquacool Multi 500?
Which are Aquacool Multi 500 UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Aquacool Multi 500 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:
- EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
- CAMPHOR, (-)- (UNII: 213N3S8275)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- WITCH HAZEL (UNII: 101I4J0U34)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
What is the NDC to RxNorm Crosswalk for Aquacool Multi 500?
- RxCUI: 259150 - menthol 3 % Topical Gel
- RxCUI: 259150 - menthol 0.03 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".