Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 63736-0013-30 recalled?

Monistat 1 Combination Pack · 1 KIT in 1 PACKAGE, COMBINATION (63736-013-30) * 1 SUPPOSITORY in 1 POUCH * 9 g in 1 TUBE

Yes — this exact package was recalled

1 FDA recall names the code 63736-0013-30 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
Miconazole Nitrate
Form
Kit
Labeler
Insight Pharmaceuticals LLC
Type
Human OTC Drug
Product code
63736-0013

Recalls naming this package

Class III · Low risk

Monistat 1 Simple Cure

Marketed without an approved NDA/ANDA: The distributed units of Monistat 1 Simple Cure include only the 1200 mg vaginal suppository; the approved NDA requires both a 1200 mg vaginal suppository and the 2% topical cream.

Terminated Unapproved drug Medtech Products, Inc. NDC 63736-013-30 D-1077-2015

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler