83732-0110 NDC - NGA ALCOHOL WIPES SANDSTONE ()

Drug Information

  • Product NDC: 83732-0110
  • Proprietary Name: NGA ALCOHOL WIPES SANDSTONE
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: NEVER GO ALONE
Product Type:
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date:10/5/2023

Package Information

No. Package Code Package Description Billing Unit
183732-0110-127 g in 1 PACKET (83732-0110-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC83732-0110The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAMENGA ALCOHOL WIPES SANDSTONEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/5/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED DRUG OTHERProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMENEVER GO ALONEThe translation of the route code submitted by the firm, indicating route of administration.

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This page was last updated on: 11/21/2025