NDC 69388-4001 Huitomi Slimming Sports

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:
69388-4001
Proprietary Name:
Huitomi Slimming Sports
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Code:
69388
Start Marketing Date: [9]
11-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 69388-4001?

The NDC code 69388-4001 is assigned by the FDA to the product Huitomi Slimming Sports which is product labeled by Lancell Bio Co., Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69388-4001-1 500 ml in 1 bottle . 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 Huitomi Slimming Sports?

This product is only used to manage your site, such as fat or forearm and thigh and can be applied to all parts of the body except the face and chest, but use the small sensitive area.Squeeze the required amount of gel in the palm when applied to the skin after 2 or 3 minutes and cool or warm feeling occurs; we recommend you so sweaty moderate exercise to the body as possible. After applying the gel is also recommended to use the sauna or electric massager aids such as hula hoops.If using this product on part that use a lot of muscle or joint before or after exercise prevent arthralgia and myalgia or restore tired muscle and joint rapidly

Which are Huitomi Slimming Sports UNII Codes?

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

Which are Huitomi Slimming Sports 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".