Drugplain

IMODIUM Multi-Symptom Relief 125 mg/1

loperamide hydrochloride and dimethicone · TABLET · Kenvue Brands LLC

No Recall History
Plain English

IMODIUM Multi-Symptom Relief is a tablet containing loperamide hydrochloride and dimethicone at 125 mg/1, taken oral. Manufactured by Kenvue Brands LLC.

Key Facts

Brand Name
IMODIUM Multi-Symptom Relief
Generic Name
loperamide hydrochloride and dimethicone
NDC Code (Product)
50580-338
Manufacturer
Kenvue Brands LLC
Strength
125 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
NDA021140
Marketing Start
07/01/2008

Recall History

No Recall History

Frequently Asked Questions

What is IMODIUM Multi-Symptom Relief used for?

IMODIUM Multi-Symptom Relief contains loperamide hydrochloride and dimethicone. It is a tablet taken oral. Consult your doctor for specific uses.

Is IMODIUM Multi-Symptom Relief a controlled substance?

IMODIUM Multi-Symptom Relief is not classified as a controlled substance by the DEA.

What is the generic name for IMODIUM Multi-Symptom Relief?

The generic name for IMODIUM Multi-Symptom Relief is loperamide hydrochloride and dimethicone. There are no other listed brand versions of loperamide hydrochloride and dimethicone.

What is the NDC code for IMODIUM Multi-Symptom Relief 125 mg/1?

The NDC (National Drug Code) for IMODIUM Multi-Symptom Relief 125 mg/1 is 50580-338, listed by Kenvue Brands LLC.

Product NDC

50580-338

Package NDC

50580-338-06

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)