Tamper Evident
Do not use this product if metal seal under the tube cap is missing or broken.
Pleo Alb
FDA Label NDC 60681-0104
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 Alb (NDC 60681-0104). 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 tamper evident, active ingredients, inactive ingredients, indications, dosage, warning, principal display panel - 30 g ointment carton, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients
1 g ointment contains; 0,1 g candida albicans 3x.
Inactive Ingredients
Cocoate magnesium sulfate, glycerylmonostearate, lactic acid, lanolin alcohol, polyglyceryl-3, propylene glycol, water.
Indications
For temporary relief of minor irritation, itching or soreness associated with Candida albicans yeast infections.
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.
Principal Display Panel - 30 G Ointment Carton
Pleo™ Alb
OINTMENT 3X
for topical
use only
Homeopathic
Antifungal
Medicine
Indications: For
temporary relief of
minor irritation,
itching or soreness
associated with
Candida albicans
yeast infections.
ORIGINAL ENDERLEIN
1.05 oz (30g)
Principal Display Panel (30 g Ointment Carton)
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