84894-018 NDC - ALOE VERA SOOTHING AND MOISTURE SERUM ()

Drug Information

  • Product NDC: 84894-018
  • Proprietary Name: Aloe Vera Soothing And Moisture Serum
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: Yiwu Ziqiu Import Export Co Ltd
Product Type:
FDA Application Number: M016
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:1/11/2025
End Marketing Date:1/11/2031

Package Information

No. Package Code Package Description Billing Unit
184894-018-015 mL in 1 BOTTLE (84894-018-01)
284894-018-0215 mL in 1 BOTTLE (84894-018-02)
384894-018-0330 mL in 1 BOTTLE (84894-018-03)
484894-018-0450 mL in 1 BOTTLE (84894-018-04)
584894-018-05100 mL in 1 BOTTLE (84894-018-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC84894-018This is the date that the labeler indicates was the start of its marketing of the drug product.
PROPRIETARY NAMEAloe Vera Soothing And Moisture SerumThis is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
START MARKETING DATE1/11/2025Product 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.
END MARKETING DATE1/11/2031 
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 NUMBERM016 
LABELER NAMEYiwu Ziqiu Import Export Co LtdName of Company corresponding to the labeler code segment of the Product NDC.

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

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