75708-7502 NDC - DR. WONJIN HAND SAFER SANIGEL ()

Drug Information

Product NDC: 75708-7502

Proprietary Name: DR. WONJIN Hand Safer Sanigel

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: BEAUTY SKIN.CO.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/10/2020

Package Information

No. Package Code Package Description Billing Unit
175708-7502-250 POUCH in 1 BOX (75708-7502-2) / 2 mL in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC75708-7502The 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 NAMEDR. WONJIN Hand Safer SanigelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/10/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBEAUTY SKIN.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: 2/1/2023