NDC 52862-130 Antibacterial Ocean Fresh

NDC Product Code 52862-130

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 generic name of Antibacterial Ocean Fresh is . The product's dosage form is and is administered via form.

Labeler Name: International Wholesale, Inc.

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)

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%




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


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.


  • 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.