NDC 76250-123 Antibacterial

NDC Product Code 76250-123

NDC CODE: 76250-123

Proprietary Name: Antibacterial 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.

NDC Code Structure

NDC 76250-123-04

Package Description: 4 BOTTLE, PLASTIC in 1 CARTON > 3.78 kg in 1 BOTTLE, PLASTIC (76250-123-01)

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

NDC Product Information

Antibacterial with NDC 76250-123 is a product labeled by Seatex Ltd. The product's dosage form is and is administered via form. The RxNorm Crosswalk for this NDC code indicates a single RxCUI concept is associated to this product: 1150812.

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 LAURETH SULFATE (UNII: BPV390UAP0)
  • LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)
  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • COCO GLUCOSIDE (UNII: ICS790225B)
  • GLYCERYL MONOOLEATE (UNII: 4PC054V79P)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • DMDM HYDANTOIN (UNII: BYR0546TOW)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Labeler Information

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

Labeler Name: Seatex Ltd
Labeler Code: 76250
Start Marketing Date: 10-14-2011 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: 12-31-2017 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.

Antibacterial Product Label Images

Antibacterial 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

Drug Facts

Active Ingredient................PurposeChloroxylenol 0.40%................Antibacterial

Uses

For hand washing to decrease bacteria on the skin.

Warnings

For external use only.

Dosage & Administration

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Otc - Stop Use

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Pump into hands, wet as needed.Lather vigorously for at least 15 secondsWash skin, rinse thoroughly and dry.

Inactive Ingredients

WATER, SODIUM LAURETH SULFATE,LAURYL GLUCOSIDE,COCAMIDOPROPYL BETAINE, PROPYLENE GLYCOL,COCO GLUCOSIDE,GLYCERYL MONOOLEATE,SODIUM CHLORIDE,DMDM HYDANTOIN,FD and C BLUE # 1,FRAGRANCE

Use In Specific Populations

FOR INDUSTRIAL USE ONLY

* Please review the disclaimer below.