NDC 78232-005 Gr Arthritis Pain Relief Roll-on 1500 Mg
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 78232-005?
What are the uses for Gr Arthritis Pain Relief Roll-on 1500 Mg?
Which are Gr Arthritis Pain Relief Roll-on 1500 Mg UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Gr Arthritis Pain Relief Roll-on 1500 Mg 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:
- OENOTHERA BIENNIS FLOWERING TOP (UNII: I3Z7321G2F)
- EQUISETUM ARVENSE WHOLE (UNII: 73DM367W4P)
- HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)
- WATER (UNII: 059QF0KO0R)
- CARTHAMUS TINCTORIUS (SAFFLOWER) OLEOSOMES (UNII: 9S60Q72309)
- BLACK COHOSH (UNII: K73E24S6X9)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- CANNABIDIOL (UNII: 19GBJ60SN5)
- SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)
- BENTONITE (UNII: A3N5ZCN45C)
- STELLARIA MEDIA (UNII: 2H03479QVR)
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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".