NDC 43689-0026 Db Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 43689-0026?
What are the uses for Db Pain Relieving?
Which are Db Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW)
- PSEUDOGNAPHALIUM OBTUSIFOLIUM (UNII: 36XQ854NWW) (Active Moiety)
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
Which are Db Pain Relieving 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:
- WATER (UNII: 059QF0KO0R)
- CANOLA OIL (UNII: 331KBJ17RK)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- OCTYL STEARATE (UNII: 772Y4UFC8B)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- TROLAMINE (UNII: 9O3K93S3TK)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- STEARETH-10 PHOSPHATE (UNII: 0B25H7PFT3)
- STEARETH-21 (UNII: 53J3F32P58)
- CETETH-20 PHOSPHATE (UNII: 921FTA1500)
- STEARIC ACID D7 (UNII: T3B081197X)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- PEG-100 STEARATE (UNII: YD01N1999R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- XANTHAN GUM (UNII: TTV12P4NEE)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CARBOMER 940 (UNII: 4Q93RCW27E)
- IMIDUREA (UNII: M629807ATL)
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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".