50260-200 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 50260-200

Proprietary Name: HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Fercy Personal Care Products Co Limited
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2010

Package Information

No. Package Code Package Description Billing Unit
150260-200-015 mL in 1 BOTTLE, PLASTIC (50260-200-01)
250260-200-028 mL in 1 BOTTLE, PLASTIC (50260-200-02)
350260-200-0310 mL in 1 BOTTLE, PLASTIC (50260-200-03)
450260-200-0420 mL in 1 BOTTLE, PLASTIC (50260-200-04)
550260-200-0530 mL in 1 BOTTLE, PLASTIC (50260-200-05)
650260-200-0650 mL in 1 BOTTLE, PLASTIC (50260-200-06)
750260-200-0760 mL in 1 BOTTLE, PLASTIC (50260-200-07)
850260-200-08100 mL in 1 BOTTLE, PLASTIC (50260-200-08)
950260-200-09120 mL in 1 BOTTLE, PLASTIC (50260-200-09)
1050260-200-10240 mL in 1 BOTTLE, PLASTIC (50260-200-10)
1150260-200-11360 mL in 1 BOTTLE, PLASTIC (50260-200-11)
1250260-200-12500 mL in 1 BOTTLE, PLASTIC (50260-200-12)
1350260-200-131000 mL in 1 BOTTLE, PLASTIC (50260-200-13)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50260-200The 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 DATE2/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEFercy Personal Care Products Co LimitedName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 7/3/2020