NDC 43689-0040 Foot Pain Relieving
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43689 - The Magni Group Inc
- 43689-0040 - Foot Pain Relieving
Product Packages
NDC Code 43689-0040-1
Package Description: 85 g in 1 BOTTLE, SPRAY
Product Details
What is NDC 43689-0040?
What are the uses for Foot Pain Relieving?
Which are Foot Pain Relieving UNII Codes?
The UNII codes for the active ingredients in this product are:
- APIS MELLIFERA (UNII: 7S82P3R43Z)
- APIS MELLIFERA (UNII: 7S82P3R43Z) (Active Moiety)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q)
- GELSEMIUM SEMPERVIRENS ROOT (UNII: 639KR60Q1Q) (Active Moiety)
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57)
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF (UNII: BGI20Z6M57) (Active Moiety)
Which are Foot 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:
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SORBIC ACID (UNII: X045WJ989B)
- GLYCERIN (UNII: PDC6A3C0OX)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- CANOLA OIL (UNII: 331KBJ17RK)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- PANTHENOL (UNII: WV9CM0O67Z)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- MENTHOL (UNII: L7T10EIP3A)
- WATER (UNII: 059QF0KO0R)
* 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".