NDC 72006-002 - KEEVA 3 IN 1 ACNE TREATMENT

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 72006-002
Package NDCs from labels: 72006-002-00
Manufacturer: COB Ecommerce Empire LLC
Effective date: 2019-08-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
KEEVA 3 IN 1 ACNE TREATMENT - COB Ecommerce Empire LLC	COB Ecommerce Empire LLC	2019-08-26	HUMAN OTC DRUG LABEL

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 144 of 144 · 2,864 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
MG217 Psoriasis	SALICYLIC ACID	Wisconsin Pharmacal Company	2d2c2ab3-7c9e-1d09-e054-00144ff8d46c	2016-03-03	Warnings	Exact identifier unii: O414PZ4LPZ
Antacid	ALUMINUM HYDROXIDE, MAGNESIUM HYDROXIDE AND SIMETHICONE	Safeway	d36b56a4-06f0-47ff-8add-4c327d60be22	2016-01-21	Warnings	Exact identifier unii: 92RU3N3Y1O
Gas Relief	SIMETHICONE	Safeway	14a9fb00-707a-4b55-a060-82ad53a806e3	2016-01-08	Warnings	Exact identifier unii: 92RU3N3Y1O
SKIN MEDICA Purifying Foaming Wash	SALICYLIC ACID	Allergan, Inc.	064d9e2b-077f-4229-b653-666fc5479ae2	2013-03-01	Warnings	Exact identifier unii: O414PZ4LPZ

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.