NDC 29500-9038 Personal Care Antibacterial Hand

  1. Labeler Index
  2. Personal Care Products, Llc
  3. NDC: 29500-9038 Personal Care Antibacterial Hand

NDC Product Code 29500-9038

NDC CODE: 29500-9038

Proprietary Name: Personal Care Antibacterial Hand 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

  • 29500 - Personal Care Products, Llc
    • 29500-9038 - Personal Care Antibacterial Hand

NDC 29500-9038-6

Package Description: 221 mL in 1 BOTTLE, PUMP

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

NDC Product Information

Personal Care Antibacterial Hand with NDC 29500-9038 is a product labeled by Personal Care Products, Llc. The generic name of Personal Care Antibacterial Hand is . The product's dosage form is and is administered via form.

Labeler Name: Personal Care Products, Llc

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)
  • AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
  • AMMONIUM CHLORIDE (UNII: 01Q9PC255D)
  • LAURIC DIETHANOLAMIDE (UNII: I29I2VHG38)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • 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: Personal Care Products, Llc
Labeler Code: 29500
Start Marketing Date: 04-11-2011 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".

* Please review the disclaimer below.

Personal Care Antibacterial Hand Product Label Images

Personal Care Antibacterial Hand 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 0.2%

Purpose

Antibacterial

Uses

For handwashing to decrease bacteria on the skin

Warnings

For external use only

When Using This Product

Avoid contact with eyes. In case of eye contact, flush with water.

Stop Use And Ask A Doctor

If irritation and redness develops

Keep Out Of Reach Of Children

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

Directions

Pump into handslather vigorously for at least 15 secondsrinse and dry thoroughly

Inactive Ingredients

Water (aqua), ammonium lauryl sulfate, ammonium chloride, lauramide DEA, DMDM hydantoin, fragrance, citric acid, tetrasodium EDTA, yellow #5, red #40

* Please review the disclaimer below.