70939-004 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 70939-004

Proprietary Name: Hand sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dongguang Shuoguo Silicone Products Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/6/2020

Package Information

No. Package Code Package Description Billing Unit
170939-004-01200 BOTTLE in 1 BOX (70939-004-01) / 30 mL in 1 BOTTLE
270939-004-02200 BOTTLE in 1 BOX (70939-004-02) / 40 mL in 1 BOTTLE
370939-004-03200 BOTTLE in 1 BOX (70939-004-03) / 50 mL in 1 BOTTLE
470939-004-04200 BOTTLE in 1 BOX (70939-004-04) / 60 mL in 1 BOTTLE
570939-004-05150 BOTTLE in 1 BOX (70939-004-05) / 100 mL in 1 BOTTLE
670939-004-06100 BOTTLE in 1 BOX (70939-004-06) / 120 mL in 1 BOTTLE
770939-004-07100 BOTTLE in 1 BOX (70939-004-07) / 150 mL in 1 BOTTLE
870939-004-0848 BOTTLE in 1 BOX (70939-004-08) / 250 mL in 1 BOTTLE
970939-004-0924 BOTTLE in 1 BOX (70939-004-09) / 500 mL in 1 BOTTLE
1070939-004-10400 BOTTLE in 1 BOX (70939-004-10) / 15 mL in 1 BOTTLE
1170939-004-118 BOX in 1 CARTON (70939-004-11) / 36 BOTTLE in 1 BOX / 30 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70939-004The 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 DATE5/6/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDongguang Shuoguo Silicone 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: 2/1/2023