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  4. NDC Product Code: 77177-002 Scb-hs-70c

NDC 77177-002 Scb-hs-70c

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 77177-002?
  4. Scb-hs-70c Uses
  5. Active Ingredients UNII Codes
  6. 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:
77177-002
Proprietary Name:
Scb-hs-70c
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Smk Holdings Llc
Labeler Code:
77177
Product Label ID:
a75b92e8-0455-d568-e053-2a95a90a6a4f
Start Marketing Date: [9]
03-30-2020
Listing Expiration Date: [11]
12-31-2021
Exclude Flag: [12]
I
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Code Structure Chart

Product Details

What is NDC 77177-002?

The NDC code 77177-002 is assigned by the FDA to the product Scb-hs-70c which is product labeled by Smk Holdings Llc. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 77177-002-01 .06 l in 1 bottle , 77177-002-02 .12 l in 1 bottle , 77177-002-03 3.785 l in 1 bottle , 77177-002-04 1.89 l in 1 jug , 77177-002-05 1.89 l in 1 jug , 77177-002-06 .06 l 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 Scb-hs-70c?

Place enough product on hands to cover all surfaces. Rub hands together until dry.Supervise children under 6 years of age when using this product to avoid swallowing.

Which are Scb-hs-70c UNII Codes?

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

Which are Scb-hs-70c 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".