75622-622 NDC - DEYO ()

Drug Information

  • Product NDC: 75622-622
  • Proprietary Name: DEYO
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Henan Yeesain Health Technology Co., Ltd.
Product Type:
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:5/1/2020

Package Information

No. Package Code Package Description Billing Unit
175622-622-1010 NOT APPLICABLE in 1 POUCH (75622-622-10) / 6.2 mL in 1 NOT APPLICABLE
275622-622-2040 NOT APPLICABLE in 1 POUCH (75622-622-20) / 6.2 mL in 1 NOT APPLICABLE
375622-622-3050 NOT APPLICABLE in 1 CANISTER (75622-622-30) / 50 mL in 1 NOT APPLICABLE
475622-622-4080 NOT APPLICABLE in 1 CANISTER (75622-622-40) / 80 mL in 1 NOT APPLICABLE
575622-622-50100 NOT APPLICABLE in 1 CANISTER (75622-622-50) / 100 mL in 1 NOT APPLICABLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC75622-622The 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 NAMEDEYOThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2020This 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 NUMBERpart333AThis 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 NAMEHenan Yeesain Health Technology Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/4/2025

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