Acnezzol Base
FDA Label NDC 58268-013

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Solution International Inc for the product Acnezzol Base (NDC 58268-013). 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 active ingredient:, uses:, other, otc - keep out of reach of children, directions:, inactive ingredients:, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient:

Salicylic acid 1.0%

Uses:

For the treatment of acne.

Other

For external use only. Avoid contact with eyes. If contact occurs, flush thoroughly with water. This product may cause irritation. If excess irritation occurs, discontinue use. Avoid unnecessary sun exposure and use sunscreen. Allow acnezzol™ base to dry, then follow the sunscreen directions. Do not use this product if you have sensitive skin or If you are sensitive to AH As.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions:

Apply a thin layer to affected area only, In the morning and evening. For best results, apply acnezzol™ activator after acnezzol™ base. Wash hands thoroughly after application.

Inactive Ingredients:

Water, Isopropyl alcohol, Propylene glycol, Hydroxyethylcellulose, Mandelic acid, Methyloxirane, Oxirane, Sodium benzoate, FD&C Blue #1.

Dist. by: SOLUTION INTERNATIONAL, INC.

Miami Beach, FL 33140 Made in USA ©2012

Package Label.Principal Display Panel

Principal Display Panel – Tube Label

Fast dual action
to clear skin

acnezzolbase

Eliminates acne causing bacteria

Clinical results without a prescription

Gentle enough for everyday use

Dermatologist Recommended
FDA REGISTERED
MADE IN USA
NET WT. 1 OZ. (28 G)

Principal Display Panel – Tube Label (Acn00 0000 01)

Principal Display Panel – Tube Label (Acn00 0000 01)

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