90107-3623 NDC - AFTER BITE WIPE INSECT STING RELIEF ()

Drug Information

Product NDC: 90107-3623

Proprietary Name: After Bite Wipe Insect Sting Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Adventure Ready Brands
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/1/2020

Package Information

No. Package Code Package Description Billing Unit
190107-3623-11000 mg in 1 PACKAGE (90107-3623-1)
290107-3623-2100 PACKET in 1 BOX (90107-3623-2) / 1000 mg in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC90107-3623The 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 NAMEAfter Bite Wipe Insect Sting 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 DATE12/1/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAdventure Ready BrandsName 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