54162-100 NDC - BENZOIN COMPOUND TINCTURE ()

Drug Information

Product NDC: 54162-100

Proprietary Name: Benzoin Compound Tincture

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Geritrex LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/31/2015

Package Information

No. Package Code Package Description Billing Unit
154162-100-0129 mL in 1 BOTTLE, PLASTIC (54162-100-01)ML
254162-100-0258 mL in 1 BOTTLE, PLASTIC (54162-100-02)ML
354162-100-04118 mL in 1 BOTTLE, PLASTIC (54162-100-04)ML

NDC Record

Field Name Field Value Definition
PRODUCT NDC54162-100The 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 NAMEBenzoin Compound TinctureThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/31/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGeritrex LLCName 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