84764-702 NDC - IQ SHIELD PRO BATH PRODUCT ()

Drug Information

  • Product NDC: 84764-702
  • Proprietary Name: iq shield pro bath product
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: AIKM Product Corp
Product Type:
FDA Application Number: M020
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/8/2025
End Marketing Date:1/8/2025

Package Information

No. Package Code Package Description Billing Unit
184764-702-70100 g in 1 PACKAGE (84764-702-70)

NDC Record

Field Name Field Value Definition
PRODUCT NDC84764-702The 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 NAMEiq shield pro bath productThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/8/2025The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
END MARKETING DATE1/8/2025The translation of the route code submitted by the firm, indicating route of administration.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM020Product 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 NAMEAIKM Product CorpName 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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