NDC 52862-130 Antibacterial Ocean Fresh

NDC Product Code 52862-130

NDC CODE: 52862-130

Proprietary Name: Antibacterial Ocean Fresh 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

  • 52862 - International Wholesale, Inc.

NDC 52862-130-03

Package Description: 3 CARTON in 1 PACKET > 90 g in 1 CARTON

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

NDC Product Information

Antibacterial Ocean Fresh with NDC 52862-130 is a product labeled by International Wholesale, Inc.. 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: 1426615.

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.

  • SODIUM COCOATE (UNII: R1TQH25F4I)
  • SODIUM PALMATE (UNII: S0A6004K3Z)
  • WATER (UNII: 059QF0KO0R)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • SODIUM CHLORIDE (UNII: 451W47IQ8X)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)

Product Labeler Information

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

Labeler Name: International Wholesale, Inc.
Labeler Code: 52862
Start Marketing Date: 07-15-2015 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".

* Please review the disclaimer below.

Antibacterial Ocean Fresh Product Label Images

Antibacterial Ocean Fresh 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

Triclocarban 0.30%

Purpose

Antibacterial

Uses

  • Helps reduce bacteria on the skin that could cause disease.Recommended for repeated use

Warnings

For external use only

When Using This Product:

Do not use in or near the eyes. In case of eye contact, rinse eyes thoroughly with water.

Stop Use And Ask A Doctor If:

Irritation and redness develops and lasts more than 72 hours.

Keeps Out Of Reach Of Children.

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

Directions

  • Wet bar with waterLather vigorously and wash skinRinse and dry thoroughly

Other Information

  • Store below 110° F (43° C)May discolor certain fabrics or surfaces

Inactive Ingredients

Sodium Cocoate, Sodium Palmate, Water, Glycerin, Sodium Chloride, Titanium Dioxide, BHT, Fragrance

* Please review the disclaimer below.