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  4. NDC Product Code: 57815-010 First Aid Shot Therapy Allergy Relief

NDC 57815-010 First Aid Shot Therapy Allergy Relief

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 57815-010?
  5. First Aid Shot Therapy Allergy Relief Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
57815-010
Proprietary Name:
First Aid Shot Therapy Allergy Relief
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
First Aid Beverages, Inc.
Labeler Code:
57815
Product Label ID:
af7c4f91-a3d8-4c16-b82c-7e9867986d0b
Start Marketing Date: [9]
07-01-2016
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Flavor(s):
MANGO (C73400)
PEACH (C73407)

Code Structure Chart

Product Details

What is NDC 57815-010?

The NDC code 57815-010 is assigned by the FDA to the product First Aid Shot Therapy Allergy Relief which is product labeled by First Aid Beverages, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 57815-010-01 1 bottle, plastic in 1 carton / 40 ml in 1 bottle, plastic. 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 First Aid Shot Therapy Allergy Relief?

Adults and children 12 years and over: swallow the contents of one bottlerepeat every 4-6 hours while symptoms persist, or as directed by doctordo not take more than 6 bottles in 24 hoursChildren under 12 years: Do not use

Which are First Aid Shot Therapy Allergy Relief UNII Codes?

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

  • DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40)
  • DIPHENHYDRAMINE (UNII: 8GTS82S83M) (Active Moiety)

Which are First Aid Shot Therapy Allergy Relief 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:

What is the NDC to RxNorm Crosswalk for First Aid Shot Therapy Allergy Relief?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 1049884 - diphenhydrAMINE HCl 50 MG in 40 mL Oral Solution
  • RxCUI: 1049884 - diphenhydramine hydrochloride 1.25 MG/ML Oral Solution
  • RxCUI: 1049884 - diphenhydramine hydrochloride 50 MG per 40 ML Oral Solution

* 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".