NDC 70694-0002 Claon All 4 Cleanser

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:
70694-0002
Proprietary Name:
Claon All 4 Cleanser
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Labeler Code:
70694
Start Marketing Date: [9]
01-24-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
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Product Details

What is NDC 70694-0002?

The NDC code 70694-0002 is assigned by the FDA to the product Claon All 4 Cleanser which is product labeled by Inc Mbg. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70694-0002-1 500 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 Claon All 4 Cleanser?

Hair After soaking hair with warm water, pour a moderate amount onto the hands, gently massage the product onto the scalp and hair, and then wash out the product thoroughly. Shaving With warm water, wet the area that will be shaved, pour a moderate amount and create a foam, shave, and then wash out the product thoroughly. Body Take a moderate amount of product and put onto a shower puff or sponge, massage the entire body, and then wash out the product thoroughly. Foam Cleanser Wet the entire face, pour a moderate amount and create a foam, gently massage the face and then wash out the product thoroughly with warm water

Which are Claon All 4 Cleanser UNII Codes?

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

Which are Claon All 4 Cleanser 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".