NDC 43689-0039 Db Foot Pain Relieving
Apis Mellifica, Gelsemium Sempervirens, Gnaphalium
NDC Product Code 43689-0039
Proprietary Name: Db Foot Pain Relieving What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name: Apis Mellifica, Gelsemium Sempervirens, Gnaphalium What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
NDC Code Structure
- 43689 - The Magni Group Inc
- 43689-0039 - Db Foot Pain Relieving
NDC 43689-0039-1
Package Description: 85 g in 1 BOTTLE, SPRAY
NDC Product Information
Db Foot Pain Relieving with NDC 43689-0039 is a a human over the counter drug product labeled by The Magni Group Inc. The generic name of Db Foot Pain Relieving is apis mellifica, gelsemium sempervirens, gnaphalium. The product's dosage form is spray and is administered via topical form.
Labeler Name: The Magni Group Inc
Dosage Form: Spray - A liquid minutely divided as by a jet of air or steam.
Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Db Foot Pain Relieving Active Ingredient(s)
What is the Active Ingredient(s) List?This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
- PSEUDOGNAPHALIUM LUTEOALBUM LEAF 3 [hp_X]/100g
- APIS MELLIFERA 3 [hp_X]/100g
- GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/100g
Inactive Ingredient(s)
About the Inactive Ingredient(s)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.
- WATER (UNII: 059QF0KO0R)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- CANOLA OIL (UNII: 331KBJ17RK)
- ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
- SORBIC ACID (UNII: X045WJ989B)
- MENTHOL (UNII: L7T10EIP3A)
- CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
- PANTHENOL (UNII: WV9CM0O67Z)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- MENTHA X PIPERITA WHOLE (UNII: 79M2M2UDA9)
- BERGAMOT OIL (UNII: 39W1PKE3JI)
- GLYCERIN (UNII: PDC6A3C0OX)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
Administration Route(s)
What are the Administration Route(s)?The translation of the route code submitted by the firm, indicating route of administration.
- Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Product Labeler Information
What is the Labeler Name?Name of Company corresponding to the labeler code segment of the Product NDC.
Labeler Name: The Magni Group Inc
Labeler Code: 43689
Marketing Category: UNAPPROVED HOMEOPATHIC - What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
Start Marketing Date: 12-29-2020 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date: 12-31-2021 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.
Exclude Flag: N 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. Values = ‘Y’ or ‘N’.
* Please review the disclaimer below.
Db Foot Pain Relieving Product Label Images
Db Foot Pain Relieving Product Labeling Information
The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.
Product Labeling Index
- Active Ingredients (In Spray) - Purpose Apis Mellifica 3X Hpus - Relieves Foot Pain Gnaphalium 3X Hpus - Relieves Foot Pain Gelsemium Sempervirens 6X Hpus - External Analgesic
- Purpose: Relieves Foot Pain External Analgesic
- Use: Temporarily Relieves Foot Pain
- Keep Out Of Reach Of Children
- Warnings: For External Use Only
- When Using This Product: - Avoid Contact With Eyes
- If Symptoms Persist For More Than 7 Days Or Worsen, Consult Your Physician
- Do Not Use On Open Wounds, Cuts, Damaged, Or Infected Skin
- Directions: - Adults And Children 12 Years Of Age And Older, Apply To All Surfaces On The Feet, Heels And Toes Up To Four Times Daily - Apply To Legs As Needed
- Other Information: - Most Beneficial When Applied After Bathing, Showering, Or A Foot Soak - The Letters "Hpus" Indicate That The Components In This Product Are Officially Monographed In The Homeopathic Pharmacopeia Of The United States - These Statements Are Supported By The Traditional Homeopathic Principles
- Inactive Ingredients: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzoic Acid, Bergamot Oil, C14-22 Alcohol/C12-20 Alkyl Glucoside, Canola Oil, Camphor Gum, Citric Acid, Ethylhexyl Stearate, Eucalyptus Oil, Glycerin, Mentha Piperita (Peppermint) Extract, Menthol, Methyl Salicylate, Panthenol, Phenoxyethanol, Sodium Hydroxide, Sorbic Acid, Tocopheryl Acetate, Water (Aqua), Xanthan Gum
Active Ingredients (In Spray) - Purpose Apis Mellifica 3X Hpus - Relieves Foot Pain Gnaphalium 3X Hpus - Relieves Foot Pain Gelsemium Sempervirens 6X Hpus - External Analgesic
NDC: 43689-0039
Purpose: Relieves Foot Pain External Analgesic
NDC: 43689-0039
Use: Temporarily Relieves Foot Pain
NDC: 43689-0039
Keep Out Of Reach Of Children
NDC: 43689-0039
Warnings: For External Use Only
NDC: 43689-0039
When Using This Product: - Avoid Contact With Eyes
NDC: 43689-0039
If Symptoms Persist For More Than 7 Days Or Worsen, Consult Your Physician
NDC: 43689-0039
Do Not Use On Open Wounds, Cuts, Damaged, Or Infected Skin
NDC: 43689-0039
Directions: - Adults And Children 12 Years Of Age And Older, Apply To All Surfaces On The Feet, Heels And Toes Up To Four Times Daily - Apply To Legs As Needed
NDC: 43689-0039
Other Information: - Most Beneficial When Applied After Bathing, Showering, Or A Foot Soak - The Letters "Hpus" Indicate That The Components In This Product Are Officially Monographed In The Homeopathic Pharmacopeia Of The United States - These Statements Are Supported By The Traditional Homeopathic Principles
NDC: 43689-0039
Inactive Ingredients: Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Benzoic Acid, Bergamot Oil, C14-22 Alcohol/C12-20 Alkyl Glucoside, Canola Oil, Camphor Gum, Citric Acid, Ethylhexyl Stearate, Eucalyptus Oil, Glycerin, Mentha Piperita (Peppermint) Extract, Menthol, Methyl Salicylate, Panthenol, Phenoxyethanol, Sodium Hydroxide, Sorbic Acid, Tocopheryl Acetate, Water (Aqua), Xanthan Gum
NDC: 43689-0039
* Please review the disclaimer below.
