Pleo Muc
FDA Label NDC 60681-1806

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sanum Kehlbeck Gmbh & Co. Kg for the product Pleo Muc (NDC 60681-1806). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding indications, dosage, warning, tamper evident, active ingredients, inactive ingredients, principal display panel - 30 g ointment carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Indications

For temporary relief of pain of bruises, sprains, swelling of joints and muscles.

Dosage

Apply thinly on the affected area 1–3 times daily.

Warning

If symptoms persist more than a few days, contact a licensed practitioner. As with any other drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before using this product.

Tamper Evident

Do not use this product if metal seal under the tube cap is missing or broken or if imprinted security strip on carton is torn.

Active Ingredients

1 g ointment contains; 0.1 g Mucor racemosus 3x.

Inactive Ingredients

lactic acid, lanolin alcohol, glycerylmonostearate, propylene glycol, polyglyceryl-3, cocoate magnesium sulfate, water.

Principal Display Panel - 30 G Ointment Carton

Pleo™ Muc
OINTMENT 3X

for topical
use only
Homeopathic
External Analgesic
Medicine

Indications: For
temporary relief of
pain of bruises,
sprains, swelling of
joints and muscles.

ORIGINAL ENDERLEIN

1.05 oz (30g)

Principal Display Panel (30 g Ointment Carton)

Principal Display Panel (30 g Ointment Carton)

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