Indications
For elimination and diuretic action.
Pleo Muc Ex
FDA Label NDC 60681-1905
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 Ex (NDC 60681-1905). 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, directions for use, dosage, ingredients, warning, tamper evident, principal display panel - 1 ml vial carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Directions For Use
Snap off top portion of sipping container. Insert glass sipping straw.
Dosage
1 SIP, once weekly, after use of Pleo™ Muc.
Ingredients
1 mL contains Mucor racemosus Anti chrondrite serum 6X, in a base of purified saline solution.
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 using this product.
Tamper Evident
Do not use this product if the glass vial is broken or if imprinted security strip on carton is torn.
Principal Display Panel - 1 Ml Vial Carton
1905-1
Pleo™ Muc EX
PORTABLE SIPS 6X
Oral Homeopathic Medicine
INDICATIONS: For elimination and di-
uretic action.
DIRECTIONS FOR USE: Snap off top
portion of sipping container. Insert glass
sipping straw.
DOSAGE: 1 SIP, once weekly, after use
of Pleo™ Muc.
INGREDIENTS: 1 mL contains Mucor
racemosus Anti chrondrite serum 6X, in a
base of purified saline solution.
convenient, disposable
single dose containers
10 doses, each 1 mL
(.03 fl oz)
Rev. 8/99
Principal Display Panel (1 mL Vial Carton)
* Please review the disclaimer below.
