NDC 66854-021 Spai-sons Acid Anti-dandruff

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:
66854-021
Proprietary Name:
Spai-sons Acid Anti-dandruff
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Spai-sons Pharamcuetical International Cosmetics
Labeler Code:
66854
Start Marketing Date: [9]
06-30-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Packages

NDC Code 66854-021-01

Package Description: 210 mL in 1 BOTTLE

NDC Code 66854-021-02

Package Description: 250 mL in 1 BOTTLE

NDC Code 66854-021-03

Package Description: 250 mL in 1 BOTTLE

Product Details

What is NDC 66854-021?

The NDC code 66854-021 is assigned by the FDA to the product Spai-sons Acid Anti-dandruff which is product labeled by Spai-sons Pharamcuetical International Cosmetics. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 66854-021-01 210 ml in 1 bottle , 66854-021-02 250 ml in 1 bottle , 66854-021-03 250 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 Spai-sons Acid Anti-dandruff?

This product is for topical application. Wash the hair with the shampoo in the shower

Which are Spai-sons Acid Anti-dandruff UNII Codes?

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

Which are Spai-sons Acid Anti-dandruff 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".