NDC 70072-001 Cocobath Waterless

NDC Product Code 70072-001

NDC CODE: 70072-001

Proprietary Name: Cocobath Waterless 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

  • 70072 - Giod Co.

NDC 70072-001-01

Package Description: 191.64 g 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

Cocobath Waterless with NDC 70072-001 is a product labeled by Giod Co.. 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: 1665365.

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.

  • COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
  • EDETATE DISODIUM (UNII: 7FLD91C86K)
  • METHYLPARABEN (UNII: A2I8C7HI9T)
  • BOMBYX MORI FIBER (UNII: 6LK42KUV6W)
  • ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)
  • ROSEMARY (UNII: IJ67X351P9)
  • GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
  • WATER (UNII: 059QF0KO0R)

Product Labeler Information

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

Labeler Name: Giod Co.
Labeler Code: 70072
Start Marketing Date: 09-05-2015 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".

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Cocobath Waterless Product Label Images

Cocobath Waterless 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

Otc - Active Ingredient

Benzalkonium Chloride 0.1%

Otc - Purpose

Antibacterial

Indications & Usage

Provide sanitizing when soap and water not availableKill or reduces 99.9 of harmful bacteria/germs

Dosage & Administration

Pump 2—3 times onto hand and rub adequately to make bubbleApply over top of head and wipe with towel after use

Warnings

For external use only.Do not use on damaged or broken skin.When using this product, keep out of eyes. Rinse with water to remove.Stop using and ask a doctor if rash occurs.

Otc - Keep Out Of Reach Of Children

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

Inactive Ingredient

Cocamidopropyl Betaine, Disodium EDTA, Methylparaben, Hydrolyzed Silk, Dimethicone Copolyol, Acorus Calamus Root Extract, Rosmarinus Officinalis (Rosemary) Extract, Dipotassium Glycyrrhizate, Lactobacillus/Aloe Barbadensis Ferment Filtrate, perfume, Water

* Please review the disclaimer below.