NDC 72036-168 Harris Teeter Foaming

NDC Product Code 72036-168

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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