NDC 65923-901 Family Care Back Pain Therapy
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65923 - United Exchange Corp
- 65923-901 - Family Care Back Pain Therapy
Product Packages
NDC Code 65923-901-37
Package Description: 1 PACKET in 1 BOX / 2 PATCH in 1 PACKET
Product Details
What is NDC 65923-901?
What are the uses for Family Care Back Pain Therapy?
Which are Family Care Back Pain Therapy UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- CAPSICUM OLEORESIN (UNII: UW86K581WY)
- CAPSICUM OLEORESIN (UNII: UW86K581WY) (Active Moiety)
Which are Family Care Back Pain Therapy 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:
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
- KAOLIN (UNII: 24H4NWX5CO)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Family Care Back Pain Therapy?
- RxCUI: 853132 - camphor 80 MG / capsicum 16 MG / menthol 24 MG Medicated Patch
- RxCUI: 853132 - camphor 80 MG / Capsicum extract 16 MG / menthol 24 MG Medicated Patch
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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".