NDC 36800-389 Severe Triple Medicated Gel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 36800 - Topco
- 36800-389 - Severe Triple Medicated Gel
Product Characteristics
Product Packages
NDC Code 36800-389-99
Package Description: 1 TUBE in 1 CARTON / 7 g in 1 TUBE
Product Details
What is NDC 36800-389?
What are the uses for Severe Triple Medicated Gel?
Which are Severe Triple Medicated Gel UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (Active Moiety)
- ZINC CHLORIDE (UNII: 86Q357L16B)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- BENZOCAINE (UNII: U3RSY48JW5)
- BENZOCAINE (UNII: U3RSY48JW5) (Active Moiety)
Which are Severe Triple Medicated Gel 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:
- PETROLATUM (UNII: 4T6H12BN9U)
- MINERAL OIL (UNII: T5L8T28FGP)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- POLYETHYLENE GLYCOL 1000 (UNII: U076Q6Q621)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- PECTIN (UNII: 89NA02M4RX)
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SACCHARIN (UNII: FST467XS7D)
What is the NDC to RxNorm Crosswalk for Severe Triple Medicated Gel?
- RxCUI: 2117335 - benzocaine 20 % / menthol 0.5 % / zinc chloride 0.15 % Oral Gel
- RxCUI: 2117335 - benzocaine 0.2 MG/MG / menthol 0.005 MG/MG / zinc chloride 0.0015 MG/MG Oral Gel
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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".