Dr.mollis
FDA Label NDC 79259-012

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Truva Seramik Kozmetik Temizlik Pazarlama Muteahhitlik Nakliyat Sanayi Ve Ticaret Ltd Sti for the product Dr.mollis (NDC 79259-012). 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 otc - keep out of reach of children, directions for use, inactive ingredients, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Keep Out Of Reach Of Children

KEEP AWAY FROM CHILDREN, FOOD and

Directions For Use

Lift lid and peel back sealing label. Pull top wipe through aperture in pack. Close lid after use to keep wipes moist.

Inactive Ingredients

Aqua, Phenoxyethanol, Aloe Barbadensis Leaf juice, Glycerin, Propylene Glycol, Cocamidopropyl Betaine, Parfum, Benzyl Alcohol, Dehydroacetic Acid.

Packaging

Image (Lb79259 012)

Image (Lb79259 012)

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