NDC 61577-8122 Hand And Wrist Pain Cream
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What is NDC 61577-8122?
What are the uses for Hand And Wrist Pain Cream?
Which are Hand And Wrist Pain Cream UNII Codes?
The UNII codes for the active ingredients in this product are:
- HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U)
- HISTAMINE (UNII: 820484N8I3) (Active Moiety)
Which are Hand And Wrist Pain Cream 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)
- WATER (UNII: 059QF0KO0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- CAMELLIA SINENSIS FLOWER (UNII: 9I2BJY2J17)
- MATRICARIA CHAMOMILLA (UNII: G0R4UBI2ZZ)
- EMU OIL (UNII: 344821WD61)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PUNICA GRANATUM SEED (UNII: 7294Z34NS7)
- SACCHARIDE ISOMERATE (UNII: W8K377W98I)
- SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRIDECETH-6 (UNII: 3T5PCR2H0C)
- VACCINIUM ANGUSTIFOLIUM WHOLE (UNII: R3538BZ1BW)
- PROPANEDIOL (UNII: 5965N8W85T)
What is the NDC to RxNorm Crosswalk for Hand And Wrist Pain Cream?
- RxCUI: 1091387 - histamine dihydrochloride 0.025 % Topical Cream
- RxCUI: 1091387 - histamine dihydrochloride 0.25 MG/ML Topical Cream
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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".