NDC 43136-102 Avon Hexashield Pain Relief For Muscle, Back And Joint Cream

Camphor, Menthol, Methyl Salicylate

NDC Product Code 43136-102

NDC Code: 43136-102

Proprietary Name: Avon Hexashield Pain Relief For Muscle, Back And Joint Cream 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: Camphor, Menthol, Methyl Salicylate 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

  • 43136 - Tai Guk Pharm. Co., Ltd.
    • 43136-102 - Avon Hexashield Pain Relief For Muscle, Back And Joint

NDC 43136-102-01

Package Description: 1 TUBE in 1 CARTON > 56.7 g in 1 TUBE

NDC Product Information

Avon Hexashield Pain Relief For Muscle, Back And Joint Cream with NDC 43136-102 is a a human over the counter drug product labeled by Tai Guk Pharm. Co., Ltd.. The generic name of Avon Hexashield Pain Relief For Muscle, Back And Joint Cream is camphor, menthol, methyl salicylate. The product's dosage form is cream and is administered via topical form.

Labeler Name: Tai Guk Pharm. Co., Ltd.

Dosage Form: Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.

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.

Avon Hexashield Pain Relief For Muscle, Back And Joint Cream 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.

  • LEVOMENTHOL 100 mg/g
  • METHYL SALICYLATE 300 mg/g
  • CAMPHOR (SYNTHETIC) 40 mg/g

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.

  • STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
  • WATER (UNII: 059QF0KO0R)
  • PETROLATUM (UNII: 4T6H12BN9U)
  • ALCOHOL (UNII: 3K9958V90M)
  • POLYSORBATE 60 (UNII: CAL22UVI4M)
  • SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
  • ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
  • POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • LANOLIN (UNII: 7EV65EAW6H)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • PROPYLPARABEN (UNII: Z8IX2SC1OH)

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: Tai Guk Pharm. Co., Ltd.
Labeler Code: 43136
FDA Application Number: part348 What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. 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: 07-31-2019 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: 12-31-2020 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.

Avon Hexashield Pain Relief For Muscle, Back And Joint Cream Product Label Images

Avon Hexashield Pain Relief For Muscle, Back And Joint Cream 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

Camphor 4 %Menthol 10 %Methyl salicylate 30 %

Purpose

Topical analgesic

Uses

  • Temporary relieves the minor aches and pains of muscles and joints associated with:simple backachearthritisstrainsbruisessprains

Warnings

For external use only.

Do Not Use

  • On wounds or damaged skinwith a heating padon a child under 12 years of age with arthritis-like conditions

Ask A Doctor Before Use If You Have

Redness over the affected area.

When Using This Product

  • Avoid contact with eyes or mucous membranesdo not banage tightly

Stop Use And Ask A Doctor If :

  • Condition worsens or symptoms persist for more than 7 dayssymptoms clear up and occur again within a few daysexcessive skin irritation occurs

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Use only as directedadults and children 12 years of age and older : apply to affected area not more than 3 to 4 times daily
  • Children under 12 years of age : ask a doctor

Other Information

  • Store at room temperature

Inactive Ingredients

Glycerin, isopropyl myristate, lanolin, methylparaben, petrolatum, polysorbate 60, potassium cetyl phosphate, propylparaben, sorbitan monostearate, stearyl alcohol water

* Please review the disclaimer below.

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