69139-001 NDC - ALCOHOL PREP PAD ()

Drug Information

Product NDC: 69139-001

Proprietary Name: Alcohol Prep Pad

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: YIWU HAODING MEDICAL CO.,LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/24/2014

Package Information

No. Package Code Package Description Billing Unit
169139-001-011 POUCH in 1 BAG (69139-001-01) / .21 mL in 1 POUCH
269139-001-022 POUCH in 1 BAG (69139-001-02) / .21 mL in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC69139-001The 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 NAMEAlcohol Prep PadThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/24/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEYIWU HAODING MEDICAL CO.,LTDName 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