75001-201 NDC - DEVOLVER PREMIUM GEL ()

Drug Information

Product NDC: 75001-201

Proprietary Name: Devolver Premium Gel

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Devolver Cosmetics Co., Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/8/2020

Package Information

No. Package Code Package Description Billing Unit
175001-201-0160 mL in 1 BOTTLE (75001-201-01)
275001-201-02100 mL in 1 BOTTLE (75001-201-02)
375001-201-03236 mL in 1 BOTTLE, PUMP (75001-201-03)
475001-201-04500 mL in 1 BOTTLE, PUMP (75001-201-04)
575001-201-053785 mL in 1 BOTTLE (75001-201-05)
675001-201-06120 mL in 1 BOTTLE (75001-201-06)
775001-201-07350 mL in 1 BOTTLE (75001-201-07)
875001-201-08300 mL in 1 BOTTLE (75001-201-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC75001-201The 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 NAMEDevolver Premium GelThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/8/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDevolver Cosmetics 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