NDC 43405-882 Eagle

NDC Product Code 43405-882

NDC 43405-882-06

Package Description: 6 PATCH in 1 PACKET

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

NDC Product Information

Eagle with NDC 43405-882 is a product labeled by Borden Company Pte Limited. The generic name of Eagle is . The product's dosage form is and is administered via form.

Labeler Name: Borden Company Pte Limited

Dosage Form: -

Product Type: 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.

  • BOSWELLIA SACRA WHOLE (UNII: 8O600AZL0W)
  • LANOLIN (UNII: 7EV65EAW6H)
  • YELLOW WAX (UNII: 2ZA36H0S2V)
  • NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
  • ZINC OXIDE (UNII: SOI2LOH54Z)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Borden Company Pte Limited
Labeler Code: 43405
Start Marketing Date: 08-01-2016 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: 12-31-2018 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: I 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.

Eagle Product Label Images

Eagle 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

Capsaicin 0.0625%Menthol 3.4%

Purpose

External AnalgesicExternal Analgesic

Uses

For the temporarily relief of minor pains and aches of muscles and joints associated with ■ simple backache ■ arthritis ■ strains■ bruises ■ sprains

Warnings

For external use only Avoid getting into the eyes or on mucous membranes. This product containsdry natural rubber which may cause allergic reactions
Caution: The Packaging of this product Contains Dry Natural Rubber

When Using This Product

■ do not appply to wounds or damaged skin ■ do not bandage tightly ■ do not use otherwise than as directed ■ do not use on children under 12 years of age with arthritis like conditions

Stop Use And Ask A Doctor If

■ condition worsens or symptoms persist for more than 7 days or clear up and occur again within a few days ■ pain persists for more than 10 days ■ redness is present

Keep Out Of Reach Of Children

To avoid accidental poisoning. In case of accidental ingestion, contact a doctor or Poison Control Center immediately

Directions

■ remove patch from packet ■ cut patch to size ■ peel off protective backing and apply adhesive side to affected areaadults and children 2 years of age and older apply to affected area not more than 3 to 4 times dailychildren under 2 years of age do not use, consult a doctor

Other Information

■ store in a cool place away from sunlight■ keep unused plasters in the original packaging

Inactive Ingredients

Beeswax, gum resin, lanolin, rubber and zinc oxide

* Please review the disclaimer below.