NDC 64272-736 African Sea-coconut Herbal Mixture

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
64272-736
Proprietary Name:
African Sea-coconut Herbal Mixture
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
64272
Start Marketing Date: [9]
12-20-2011
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - NATURAL CHERRY FLAVOR)
LICORICE (C73397 - NATURAL LICORICE FLAVOR)

Code Structure Chart

Product Details

What is NDC 64272-736?

The NDC code 64272-736 is assigned by the FDA to the product African Sea-coconut Herbal Mixture which is product labeled by Luen Fook Medicine Sdn. Bhd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 64272-736-01 1 bottle, glass in 1 box / 177 ml in 1 bottle, glass. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for African Sea-coconut Herbal Mixture?

Use only as directedadults and children 12 years and oldertake orally 2 to 4 teaspoons (10-20mL) every 4 hours, not to exceed 24 teaspoons in 24 hours.children 6 to under 12 yearstake 1 to 2 teaspoons (5-10mL) every 4 hours, not to exceed 12 teaspoons in 24 hours.children under 6 yearsconsult a doctor before use.

Which are African Sea-coconut Herbal Mixture UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are African Sea-coconut Herbal Mixture Inactive Ingredients UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

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

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] 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.

[12] 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".