NDC 72593-155 Allg Pain Relief Fast Acting Pain
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 72593-155?
What are the uses for Allg Pain Relief Fast Acting Pain?
Which are Allg Pain Relief Fast Acting Pain UNII Codes?
The UNII codes for the active ingredients in this product are:
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (Active Moiety)
Which are Allg Pain Relief Fast Acting 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:
- METHYL GLUCOSE SESQUISTEARATE (UNII: V1YW10H14D)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
- CALCITRIOL (UNII: FXC9231JVH)
- CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ESCIN (UNII: RUU8G67GQM)
- GLUCOSAMINE SULFATE POTASSIUM CHLORIDE (UNII: 15VQ11I66N)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- METHYL GLUCETH-20 (UNII: J3QD0LD11P)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- WATER (UNII: 059QF0KO0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- SORBITAN MONOLAURATE (UNII: 6W9PS8B71J)
- TROLAMINE SALICYLATE (UNII: H8O4040BHD)
- CANNABIDIOL (UNII: 19GBJ60SN5)
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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".