Berberis
FDA Label NDC 51720-421

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Curative Power Lab Pvt Ltd for the product Berberis (NDC 51720-421). 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 - active ingredient, inactive ingredient, otc - purpose, indications & usage, dosage & administration, warnings, otc - keep out of reach of children, how supplied, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Berberis Aq. - 0.1mlCalendula - 0.1mlHydrastis Can. - 0.1mlAcid Boric - 1x 10mgZinc Oxide - 1x 5mgBorax - 1x5mgCalc. Sulph. - 1x 2mgAnt. Crude - 1x 2mg

Inactive Ingredient

Alcohol - 4.8 percent v/v

Otc - Purpose

Berberis is a flowered shrub known to aid in the care of acne, blemishes, and the smoothing of complexion. The unique combination of Berberis Antiseptic Cream helps to cleanse pores and leaves your skin feeling silky smooth.

Indications & Usage

Berberis. A natural solution for acne and blemishes.

- Cleanses Pores

-Clears Complexion

Dosage & Administration

Apply and rub onto skin as needed.

Warnings

- For external use only.

- Store in a cool, dry place.

Otc - Keep Out Of Reach Of Children

Keep out of the reach of children.

How Supplied

Berberis Antiseptic Cream is manufactured in India with the highest quality ingredients for Regranion, LLC, Charleston, SC 29403

References

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