0924-5711 NDC - FIRST AID ONLY FIRST AID/ BURN ()

Drug Information

  • Product NDC: 0924-5711
  • Proprietary Name: First Aid Only First Aid/ Burn
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Acme United Corporation
Product Type:
FDA Application Number: part348
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:4/8/2019

Package Information

No. Package Code Package Description Billing Unit
10924-5711-01.9 g in 1 PACKET (0924-5711-01)
20924-5711-026 PACKET in 1 CARTON (0924-5711-02) / .9 g in 1 PACKET
30924-5711-036 PACKET in 1 BAG (0924-5711-03) / .9 g in 1 PACKET
40924-5711-0410 PACKET in 1 CARTON (0924-5711-04) / .9 g in 1 PACKET
50924-5711-0510 PACKET in 1 CARTON (0924-5711-05) / .9 g in 1 PACKET
60924-5711-0612 PACKET in 1 CARTON (0924-5711-06) / .9 g in 1 PACKET
70924-5711-0720 PACKET in 1 CARTON (0924-5711-07) / .9 g in 1 PACKET
80924-5711-0820 PACKET in 1 CARTON (0924-5711-08) / .9 g in 1 PACKET
90924-5711-0925 PACKET in 1 CARTON (0924-5711-09) / .9 g in 1 PACKET
100924-5711-1025 PACKET in 1 CARTON (0924-5711-10) / .9 g in 1 PACKET
110924-5711-1150 PACKET in 1 CARTON (0924-5711-11) / .9 g in 1 PACKET
120924-5711-1260 PACKET in 1 CARTON (0924-5711-12) / .9 g in 1 PACKET
130924-5711-13144 PACKET in 1 CARTON (0924-5711-13) / .9 g in 1 PACKET
140924-5711-14144 PACKET in 1 CARTON (0924-5711-14) / .9 g in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC0924-5711The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEFirst Aid Only First Aid/ BurnThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/8/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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.
APPLICATION NUMBERpart348This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEAcme United CorporationName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/19/2025

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