NDC 72036-168 Harris Teeter Foaming

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  2. Harris Teeter
  3. NDC: 72036-168 Harris Teeter Foaming

NDC Product Code 72036-168

NDC CODE: 72036-168

Proprietary Name: Harris Teeter Foaming 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: 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

NDC 72036-168-08

Package Description: 222 mL in 1 BOTTLE, PUMP

NDC 72036-168-32

Package Description: 946 mL in 1 BOTTLE, PLASTIC

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

NDC Product Information

Harris Teeter Foaming with NDC 72036-168 is a product labeled by Harris Teeter. The generic name of Harris Teeter Foaming is . The product's dosage form is and is administered via form.

Labeler Name: Harris Teeter

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)
  • SODIUM POLYSTYRENE SULFONATE (UNII: 1699G8679Z)
  • DIPROPYLENE GLYCOL (UNII: E107L85C40)
  • AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • SODIUM PHOSPHATE, DIBASIC, DIHYDRATE (UNII: 94255I6E2T)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • FD&C RED NO. 4 (UNII: X3W0AM1JLX)
  • FD&C YELLOW NO. 5 (UNII: I753WB2F1M)

Product Labeler Information

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

Labeler Name: Harris Teeter
Labeler Code: 72036
Start Marketing Date: 10-07-2010 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 - INACTIVATED, the listing data was inactivated by the FDA. 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

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Harris Teeter Foaming Product Label Images

Harris Teeter Foaming 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

Triclosan 0.6%

Purpose

Antibacterial

Warnings

For external use only.

When Using This Product

- Avoid contact with eyes. If contact occurs, rinse with water.

Stop Using This Product And Ask Doctor If

- irritation or redness develops and lasts.

Keep Out Of Reach Of Children

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

Directions

Pump onto dry hands, work vigorously into a lather and rinse thoroughly.

Uses

Helps to decrease bacteria on the skin

Inactive Ingredients

Water (Aqua), Sodium Xylenesulfonate, Dipropylene Glycol, Ammonium Lauryl Sulfate, Cocamidopropyl Betaine, Fragrance(Parfum), Disodium Phosphate, Citric Acid,Yellow 5 (CI 19140), Red 40 (CI 16035).

Package Front And Back Labels

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