70648-133 NDC - OLP ANTI-ITCH ALLERGY RELIEF ()

Drug Information

Product NDC: 70648-133

Proprietary Name: OLP ANTI-ITCH ALLERGY RELIEF

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: OHIO LAB PHARMA LLC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/21/2018

Package Information

No. Package Code Package Description Billing Unit
170648-133-011 TUBE in 1 CARTON (70648-133-01) / 20 g in 1 TUBE

NDC Record

Field Name Field Value Definition
PRODUCT NDC70648-133The 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 NAMEOLP ANTI-ITCH ALLERGY RELIEFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/21/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEOHIO LAB PHARMA LLC.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