Indications
For temporary relief of pain of bruises, sprains, swelling of joints and muscles.
Pleo Muc
FDA Label NDC 60681-1805
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 60681-1805). 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, active ingredient per dose, inactive ingredients, dosage, warning, tamper evident, principal display panel - 10 suppository carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient Per Dose
0.2 g Mucor racemosus 3X.
Inactive Ingredients
hydrogenated palm kernel glycerides, lactose.
Dosage
Once daily, insert one suppository rectally at bedtime.
Warning
If symptoms persist more than a few days, contact a licensed practitioner. As with any drug, if you are pregnant or nursing a baby, seek the advice of a health care professional before taking this product.
Tamper Evident
Do not use this product if imprinted inner plastic shell is broken or if imprinted security strip on carton package is torn.
Principal Display Panel - 10 Suppository Carton
Pleo™ Muc
SUPPOSITORIES 3X
Homeopathic Analgesic Medicine
Indications: For temporary
relief of pain of bruises, sprains,
swelling of joints and muscles.
ORIGINAL ENDERLEIN
10 SUPPOSITORIES
Principal Display Panel (10 Suppositories Carton)
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