Indications
For temporary relief of pain of bruises, sprains, swelling of joints and muscles.
Pleo Sanuvis
FDA Label NDC 60681-6301
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 Sanuvis (NDC 60681-6301). 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 - 30g tube carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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 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.
Active Ingredients
1g ointment contains: 0.1g Acidum L(+) - lacticum 1X.
Inactive Ingredients
lanolin alcohol, glycerylmonostearate, propylene glycol, polyglyceryl-3, cocoate magnesium sulfate, water.
Principal Display Panel - 30G Tube Carton
Pleo® Sanuvis
Ointment 1X
for topical use only
Homeopathic
External Analgesic
Medicine
The original
SANUM®
brand remedies
Indications: For temporary
relief of pain of bruises,
sprains, swelling of joints
and muscles.
1.05 oz (30g)
Principal Display Panel (30g Tube Carton)
* Please review the disclaimer below.
