NDC 34666-020 Arnica Treatment Pack

Arnica Treatment Pack

NDC Product Code 34666-020

NDC 34666-020-01

Package Description: 1 KIT in 1 KIT * 1 TABLET in 1 BOX

NDC Product Information

Arnica Treatment Pack with NDC 34666-020 is a a human over the counter drug product labeled by Nartex Laboratorios Homeopaticos Sa De Cv. The generic name of Arnica Treatment Pack is arnica treatment pack. The product's dosage form is kit and is administered via oral; topical form.

Labeler Name: Nartex Laboratorios Homeopaticos Sa De Cv

Dosage Form: Kit - A packaged collection of related material.

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.


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.

  • LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
  • STARCH, POTATO (UNII: 8I089SAH3T)
  • TALC (UNII: 7SEV7J4R1U)
  • GELATIN (UNII: 2G86QN327L)
  • MAGNESIUM STEARATE (UNII: 70097M6I30)
  • WATER (UNII: 059QF0KO0R)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • PARAFFIN (UNII: I9O0E3H2ZE)
  • SODIUM BENZOATE (UNII: OJ245FE5EU)
  • LANOLIN (UNII: 7EV65EAW6H)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • 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.

* Please review the disclaimer below.

Arnica Treatment Pack Product Label Images

Arnica Treatment Pack 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 Ingredient (In Each Tablet)

Arnica Montana 6C HPUS**The letters "HPUS" indicate that the components in this product are officially monographed in the Homeopathic Pharmacopoeia of the United States. "C" is an homeopathic dilution. See www.nartexlabsusa.com formore information. Active ingredients are prepared in accordance with the Homeopathic Pharmacopoeia of the United States, and are therefore non-toxic and have no known side effects.

Purpose

Arnica Montana 6C HPUS* .....Anti-inflammatory

Arnica Montana TINC HPUS*.......Anti-inflammatory/Pain ReliefHamamelis virginiana TINC HPUS.....Anti-inflammatory/Pain Relief

Uses

For the temporary relief of sore muscles, bruises, sprainsProduct uses are based on Homeopathic Materia Medica not clinical tests. This product has not been clinically tested by Nartex Labs USA, Inc.

Temporary relief for the symptoms of sore muscles, bruises, and sprains. Product uses are based on Homeopathic Materia Medica not clinical tests.

Warnings

Do not use if you have an allergy or hypersensitivity to the components of the fourmal or have had a prior reaction to this product.

  • For external use only.Do notApply to wounds tor damaged skinapply over large areas of the body

Otc - Ask Doctor

  • Stop use and ask a physcian ifcondition worsenssymptoms persist for more than 7 days or clear up and occur again within a few daysrash develops.

Otc - Pregnancy Or Breast Feeding

If pregnant or breastfeeding, consult a health professional before use.

If pregnant or breast feeding, consult a health professional before use,

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Adults and children 4 yers of age and older: take 2 tablets every 6 hours, slowly dissolving in the mouthChildren under 4 years of age: consult a physician

  • Adults and children over 2 years of age: apply generously rubbing into affected area as neededchildren 2 years of age: consult a physcian

Other Information

Store in a cool and dry place.

Store at room temperature

Inactive Ingredients

Gelatin, Lactose, Magnesium stearate, Potato stach, Talc

Glycerin, Lanolin, Paraffin, Sodium benzoate, Water, White petrolatum

Other

Product of Mexico / Producto de MexicoDistributed by: Nartex Labs, USA, Inc.11711 Memorial Drive #685 Houston, TX 77024www.nartexlabsusa.com

Active Ingredients are prepared in accordance with the Homeopathic Pharmaocopoeia of the United States, and are therefore non-toxic and have no known side effects. There is no scientific evidence that the product works. Product's claims are baed only on theories of homeopathy from the 1700's that are not accepted by most modern medical experts.

Active Ingredients

Each does contains equial parts of:Anrica Montana TINC HPUS*Hamamelis virginiana TINC HPUS*

Otc - When Using

  • When using this productavoid contact with eyes or mucous membranesdo not bandage tightly

Otc - Stop Use

  • Stop use and ask a doctor ifsymptoms persist for more than 7 das or clear up and occur again within a few daysrash develops

* Please review the disclaimer below.

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