NDC 82690-402 Orabalance Breathcare
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Product Details
What is NDC 82690-402?
What are the uses for Orabalance Breathcare?
Which are Orabalance Breathcare UNII Codes?
The UNII codes for the active ingredients in this product are:
- LACTOBACILLUS GASSERI (UNII: Q66E0D2443)
- LACTOBACILLUS GASSERI (UNII: Q66E0D2443) (Active Moiety)
- LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
- LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP) (Active Moiety)
Which are Orabalance Breathcare 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CHOLECALCIFEROL (UNII: 1C6V77QF41)
- RIBOFLAVIN (UNII: TLM2976OFR)
- PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
- THIAMINE HYDROCHLORIDE (UNII: M572600E5P)
- ACACIA (UNII: 5C5403N26O)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- ISOMALTULOSE ANHYDROUS (UNII: V59P50X4UY)
- MALTITOL (UNII: D65DG142WK)
- SUCROSE (UNII: C151H8M554)
- STARCH, CORN (UNII: O8232NY3SJ)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- BIFIDOBACTERIUM BIFIDUM BGN4 (UNII: YHK9HJP3KK)
- 4'-GALACTOSYLLACTOSE (UNII: B8CW1B3F6R)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- SPEARMINT (UNII: J7I2T6IV1N)
- BIFIDOBACTERIUM LONGUM (UNII: 831AQW699W)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
- CYANOCOBALAMIN (UNII: P6YC3EG204)
- BIFIDOBACTERIUM ANIMALIS LACTIS (UNII: 5307V7XW8I)
- DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)
- ISOMALT (UNII: S870P55O2W)
- XYLITOL (UNII: VCQ006KQ1E)
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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".