NDC 43689-0040 Foot Pain Relieving

Apis Mellifica, Gelsemium Sempervirens, Gnaphalium

NDC Product Code 43689-0040

NDC 43689-0040-1

Package Description: 85 g in 1 BOTTLE, SPRAY

NDC Product Information

Foot Pain Relieving with NDC 43689-0040 is a a human over the counter drug product labeled by The Magni Group Inc. The generic name of 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.

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.

  • APIS MELLIFERA 3 [hp_X]/100g
  • GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/100g
  • PSEUDOGNAPHALIUM LUTEOALBUM LEAF 3 [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.

  • 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)

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.

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

NDC: 43689-0040

Purpose: Relieves Foot Pain External Analgesic

NDC: 43689-0040

Use: Temporarily Relieves Foot Pain

NDC: 43689-0040

Keep Out Of Reach Of Children

NDC:

Warning: For External Use Only

NDC: 43689-0040

When Using This Product: - Avoid Contact With Eyes

NDC: 43689-0040

If Symptoms Persist For More Than 7 Days Or Worsen, Consult Your Physician

NDC: 43689-0040

Do Not Use On Open Wounds, Cuts, Damaged, Or Infected Skin

NDC: 43689-0040

Directions: - Adults And Children 12 Years Of Age And Older, Apply To All Surfaces Of The Feet, Heels And Toes Up To Four Times Daily - Apply To Legs As Needed

NDC: 43689-0040

Other Information: - Most Beneficial When Applied After Bathing, Showering, Or A Foot Soak - The Letter "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: 43689-0040

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: 43689-0040

* Please review the disclaimer below.