NDC 65923-100 Family Care Thera Flex Pain
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 65923-100?
What are the uses for Family Care Thera Flex Pain?
Which are Family Care Thera Flex Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAPSAICIN (UNII: S07O44R1ZM)
- CAPSAICIN (UNII: S07O44R1ZM) (Active Moiety)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- PEPPERMINT (UNII: V95R5KMY2B) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Family Care Thera Flex Pain 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)
- CALCIUM CARBONATE (UNII: H0G9379FGK)
- NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
What is the NDC to RxNorm Crosswalk for Family Care Thera Flex Pain?
- RxCUI: 1356330 - camphor 1.48 % / capsaicin 0.0056 % / menthol 3.95 % / methyl salicylate 3.95 % / peppermint oil 1.95 % / zinc oxide 18.77 % Medicated Pad
- RxCUI: 1356330 - camphor 14.8 MG/ML / capsaicin 0.056 MG/ML / menthol 39.5 MG/ML / methyl salicylate 39.5 MG/ML / peppermint oil 19.5 MG/ML / zinc oxide 188 MG/ML Medicated Pad
- RxCUI: 1356330 - Camphor 14.8 MG/ML / Capsaicin 0.056 MG/ML / Menthol 39.5 MG/ML / methyl salicylate 39.5 MG/ML / Peppermint oil 19.5 MG/ML / ZNO 188 MG/ML Medicated Pad
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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".