NDC 69837-100 Paingo Kft
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What is NDC 69837-100?
Which are Paingo Kft UNII Codes?
The UNII codes for the active ingredients in this product are:
- LIDOCAINE (UNII: 98PI200987)
- LIDOCAINE (UNII: 98PI200987) (Active Moiety)
- PRILOCAINE (UNII: 046O35D44R)
- PRILOCAINE (UNII: 046O35D44R) (Active Moiety)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Paingo Kft 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:
- CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- WATER (UNII: 059QF0KO0R)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- CANNABIS SATIVA SEED OIL (UNII: 69VJ1LPN1S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHONDROITIN SULFATE (SHARK) (UNII: 2ZAJ1K50XH)
- GLUCONOLACTONE (UNII: WQ29KQ9POT)
- GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- STARCH, TAPIOCA (UNII: 24SC3U704I)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PROPANEDIOL (UNII: 5965N8W85T)
What is the NDC to RxNorm Crosswalk for Paingo Kft?
- RxCUI: 197877 - lidocaine 2.5 % / prilocaine 2.5 % Topical Cream
- RxCUI: 197877 - lidocaine 25 MG/ML / prilocaine 25 MG/ML Topical Cream
- RxCUI: 311500 - menthol 10 % / methyl salicylate 30 % Topical Cream
- RxCUI: 311500 - menthol 100 MG/ML / methyl salicylate 300 MG/ML Topical Cream
* Please review the disclaimer below.
[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".