NDC 76168-401 Cold Zone Pain Relieving Gel- Dg Health
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76168-401?
What are the uses for Cold Zone Pain Relieving Gel- Dg Health?
Which are Cold Zone Pain Relieving Gel- Dg Health UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Cold Zone Pain Relieving Gel- Dg Health 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:
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- BRILLIANT BLUE G (UNII: M1ZRX790SI)
- PETROLATUM (UNII: 4T6H12BN9U)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- ARCTIUM LAPPA WHOLE (UNII: 73070DU1LA)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- FRANKINCENSE (UNII: R9XLF1R1WM)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
- MELISSA OFFICINALIS LEAF (UNII: 50D2ZE9219)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TROLAMINE (UNII: 9O3K93S3TK)
- SORBIC ACID (UNII: X045WJ989B)
- WATER (UNII: 059QF0KO0R)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
What is the NDC to RxNorm Crosswalk for Cold Zone Pain Relieving Gel- Dg Health?
- RxCUI: 415974 - menthol 4 % Topical Gel
- RxCUI: 415974 - menthol 0.04 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".