NDC 17312-035 Smokers Nicotine Relief
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 17312-035?
What are the uses for Smokers Nicotine Relief?
Which are Smokers Nicotine Relief UNII Codes?
The UNII codes for the active ingredients in this product are:
- MILK THISTLE (UNII: U946SH95EE)
- MILK THISTLE (UNII: U946SH95EE) (Active Moiety)
- ST. JOHN'S WORT (UNII: UFH8805FKA)
- ST. JOHN'S WORT (UNII: UFH8805FKA) (Active Moiety)
- WOOD CREOSOTE (UNII: 3JYG22FD73)
- WOOD CREOSOTE (UNII: 3JYG22FD73) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U)
- LOBELIA INFLATA (UNII: 9PP1T3TC5U) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190)
- ASPIDOSPERMA QUEBRACHO-BLANCO BARK (UNII: 52B1340190) (Active Moiety)
- VALERIAN (UNII: JWF5YAW3QW)
- VALERIAN (UNII: JWF5YAW3QW) (Active Moiety)
Which are Smokers Nicotine Relief 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:
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- XYLITOL (UNII: VCQ006KQ1E)
- MALTITOL (UNII: D65DG142WK)
- ACACIA (UNII: 5C5403N26O)
- LACTOSE (UNII: J2B2A4N98G)
- SPEARMINT (UNII: J7I2T6IV1N)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- ISOMALT (UNII: S870P55O2W)
- STEVIA REBAUDIUNA LEAF (UNII: 6TC6NN0876)
- SORBITOL (UNII: 506T60A25R)
- SHELLAC (UNII: 46N107B71O)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
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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".