Dosage & Administration
Adults: Apply externally twice daily to properly cleaned & dried affected portion.
Children under 18 years: As prescribed by the physician.
D-acne
FDA Label NDC 69825-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Adven Biotech Private Limited for the product D-acne (NDC 69825-005). 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 dosage & administration, warnings, otc - purpose, inactive ingredient, otc - active ingredient, indications & usage, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Warnings
If symptons persist or worsen, a physician should be consulted. Keep out of reach of children. Do not use, if known sentivity to any of its ingredients exists. In case of emergency, contact a medical professional or posion control center immediately. For external use only. Replace cap tightly.
Otc - Purpose
Controls Acne
Skin Treatment
Inactive Ingredient
Alcohol content, Cream base
Otc - Active Ingredient
Berberis Aquifolium, Thuja Occidentalis, Calendula Officinalis
Indications & Usage
Treats acne, pimples, blotches, brown spots and dark discoloration of skin. Prevents suppuration.
Package Label.Principal Display Panel
Dacnecream (Dacnecream30g)
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