75138-130 NDC - AONISEN HAND SANITIZER ()

Drug Information

Product NDC: 75138-130

Proprietary Name: Aonisen Hand Sanitizer

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Henan Shizheng Pharmaceutical Technology Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/1/2020

Package Information

No. Package Code Package Description Billing Unit
175138-130-0659 mL in 1 BOTTLE, PLASTIC (75138-130-06)
275138-130-10100 mL in 1 BOTTLE, PLASTIC (75138-130-10)
375138-130-1330 mL in 1 BOTTLE, PLASTIC (75138-130-13)
475138-130-30300 mL in 1 BOTTLE, PUMP (75138-130-30)
575138-130-51500 mL in 1 BOTTLE, PUMP (75138-130-51)
675138-130-52500 mL in 1 BOTTLE, PUMP (75138-130-52)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75138-130The 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 NAMEAonisen Hand 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 DATE2/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHenan Shizheng Pharmaceutical Technology 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