71011-001 NDC - HAND SANITIZER ()

Drug Information

Product NDC: 71011-001

Proprietary Name: HAND SANITIZER

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: NingBo Huize Commodity Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/29/2016

Package Information

No. Package Code Package Description Billing Unit
171011-001-015 mL in 1 BOTTLE, PLASTIC (71011-001-01)
271011-001-028 mL in 1 BOTTLE, PLASTIC (71011-001-02)
371011-001-0310 mL in 1 BOTTLE, PLASTIC (71011-001-03)
471011-001-0415 mL in 1 BOTTLE, PLASTIC (71011-001-04)
571011-001-0520 mL in 1 BOTTLE, PLASTIC (71011-001-05)
671011-001-0630 mL in 1 BOTTLE, PLASTIC (71011-001-06)
771011-001-0750 mL in 1 BOTTLE, PLASTIC (71011-001-07)
871011-001-0860 mL in 1 BOTTLE, PLASTIC (71011-001-08)
971011-001-0980 mL in 1 BOTTLE, PLASTIC (71011-001-09)
1071011-001-10100 mL in 1 BOTTLE, PLASTIC (71011-001-10)
1171011-001-11150 mL in 1 BOTTLE, PLASTIC (71011-001-11)
1271011-001-12200 mL in 1 BOTTLE, PLASTIC (71011-001-12)
1371011-001-13250 mL in 1 BOTTLE, PLASTIC (71011-001-13)
1471011-001-14300 mL in 1 BOTTLE, PLASTIC (71011-001-14)
1571011-001-15400 mL in 1 BOTTLE, PLASTIC (71011-001-15)
1671011-001-16500 mL in 1 BOTTLE, PLASTIC (71011-001-16)
1771011-001-17600 mL in 1 BOTTLE, PLASTIC (71011-001-17)
1871011-001-18700 mL in 1 BOTTLE, PLASTIC (71011-001-18)
1971011-001-19800 mL in 1 BOTTLE, PLASTIC (71011-001-19)
2071011-001-20900 mL in 1 BOTTLE, PLASTIC (71011-001-20)
2171011-001-211000 mL in 1 BOTTLE, PLASTIC (71011-001-21)
2271011-001-222000 mL in 1 BOTTLE, PLASTIC (71011-001-22)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71011-001The 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 DATE9/29/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENingBo Huize Commodity 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