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  4. NDC Product Code: 66854-006 Spai-sons Floop C

NDC 66854-006 Spai-sons Floop C

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 66854-006?
  5. Spai-sons Floop C Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66854-006
Proprietary Name:
Spai-sons Floop C
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Spai Sons Pharmaceutical International Cosmetics
Labeler Code:
66854
Product Label ID:
3cc98e53-d4b8-415d-ab98-12cca1cc6390
Start Marketing Date: [9]
09-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
PURPLE (C48327 - LILAC)

Product Packages

NDC Code 66854-006-02

Package Description: 1 TUBE in 1 BOX / 70 g in 1 TUBE (66854-006-01)

Product Details

What is NDC 66854-006?

The NDC code 66854-006 is assigned by the FDA to the product Spai-sons Floop C which is product labeled by Spai Sons Pharmaceutical International Cosmetics. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66854-006-02 1 tube in 1 box / 70 g in 1 tube (66854-006-01). 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 Floop C?

This product is designed for use in armpit areas as may cause irritation in the area of application by the sensitivity of the user.

Which are Spai-sons Floop C UNII Codes?

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

  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M)
  • ALUMINUM CHLOROHYDRATE (UNII: HPN8MZW13M) (Active Moiety)

Which are Spai-sons Floop C 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:

* Please review the disclaimer below.

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".