50049-001 NDC - HAND SANITIZER ()

Drug Information

  • Product NDC: 50049-001
  • Proprietary Name: Hand Sanitizer
  • Non Proprietary Name:
  • Active Ingredient(s):
  • Administration Route(s):
  • Dosage Form(s):

Labeler Information

Field Name Field Value
Labeler Name: QUANZHOU BESTHOPE HOUSEHOLD PRODUCTS CO., LTD.
Product Type:
FDA Application Number: part333E
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:4/4/2020

Package Information

No. Package Code Package Description Billing Unit
150049-001-01150 BOTTLE in 1 CARTON (50049-001-01) / 45 mL in 1 BOTTLE
250049-001-02100 BOTTLE in 1 CARTON (50049-001-02) / 75 mL in 1 BOTTLE
350049-001-0324 BOTTLE in 1 CARTON (50049-001-03) / 187.5 mL in 1 BOTTLE
450049-001-0420 BOTTLE in 1 CARTON (50049-001-04) / 375 mL in 1 BOTTLE
550049-001-0518 BOTTLE in 1 CARTON (50049-001-05) / 750 mL in 1 BOTTLE
650049-001-06200 BOTTLE in 1 CARTON (50049-001-06) / 22.5 mL in 1 BOTTLE
750049-001-07150 BOTTLE in 1 CARTON (50049-001-07) / 37.5 mL in 1 BOTTLE
850049-001-0824 BOTTLE in 1 CARTON (50049-001-08) / 112.5 mL in 1 BOTTLE
950049-001-0924 BOTTLE in 1 CARTON (50049-001-09) / 135 mL in 1 BOTTLE
1050049-001-1024 BOTTLE in 1 CARTON (50049-001-10) / 150 mL in 1 BOTTLE
1150049-001-1124 BOTTLE in 1 CARTON (50049-001-11) / 225 mL in 1 BOTTLE
1250049-001-1224 BOTTLE in 1 CARTON (50049-001-12) / 367.5 mL in 1 BOTTLE
1350049-001-1312 BOTTLE in 1 CARTON (50049-001-13) / 900 mL in 1 BOTTLE
1450049-001-1412 BOTTLE in 1 CARTON (50049-001-14) / 1500 mL in 1 BOTTLE
1550049-001-154 BOTTLE in 1 CARTON (50049-001-15) / 2835 mL in 1 BOTTLE
1650049-001-164 BOTTLE in 1 CARTON (50049-001-16) / 3750 mL in 1 BOTTLE
1750049-001-172 BOTTLE in 1 CARTON (50049-001-17) / 7500 mL in 1 BOTTLE
1850049-001-181 BOTTLE in 1 CARTON (50049-001-18) / 18750 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50049-001The 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 NAMEHand SanitizerThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/4/2020This 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 NUMBERpart333EThis 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 NAMEQUANZHOU BESTHOPE HOUSEHOLD PRODUCTS 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: 7/4/2025

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