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  4. NDC Product Code: 58826-704 Coats Aloe Analgesic

NDC 58826-704 Coats Aloe Analgesic

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 58826-704?
  5. Coats Aloe Analgesic 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:
58826-704
Proprietary Name:
Coats Aloe Analgesic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tychasis Corporation
Labeler Code:
58826
Product Label ID:
135157a2-cd0d-61a8-e054-00144ff8d46c
Start Marketing Date: [9]
09-29-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)

Code Structure Chart

Product Details

What is NDC 58826-704?

The NDC code 58826-704 is assigned by the FDA to the product Coats Aloe Analgesic which is product labeled by Tychasis Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 58826-704-08 237 g in 1 bottle, dispensing , 58826-704-33 976 g in 1 bottle, dispensing . 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 Coats Aloe Analgesic?

ADULTS AND CHILDREN 12 YEARS OF AGE AND OLDER: apply to affected areas no more than 3-4 times daily.CHILDREN UNDER 12 YEARS OF AGE: consult a physician.

Which are Coats Aloe Analgesic UNII Codes?

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

Which are Coats Aloe Analgesic 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".