Sea Breeze Actives Clear-pore Astringent
FDA Label NDC 41595-3020

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Idelle Labs, Ltd for the product Sea Breeze Actives Clear-pore Astringent (NDC 41595-3020). 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, purpose, uses, warnings, when using this product, keep out of reach of children., flammable,, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Salicylic acid 2%

Purpose

Acne medication

Uses

  • for the treatment of acne
  • clears blackheads

Warnings

For external use only.

When Using This Product

  • and other topical acne medication at the same time or immediately following use of this product, dryness or irritation of the skin may be increased. If this occurs, only one medication should be used unless directed by a doctor.

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Flammable,

keep away from open fire or flame.

Directions

  • clean skin thoroughly before applying medication.
  • moisten a cotton ball and smooth the cotton ball over your face one to three times daily.

Inactive Ingredients

Benzoic acid, camphor, clove (eugenia caryophyllus) oil, eucalyptus globulus oil, Ext. violet 2, fragrance, glycerin, methyl propanediol, PPG-12-buteth-16, SD alcohol 40-B, sodium benzoate, water.

Questions Or Comments?

1-800-487-7273 or visit us at www.seabreezeclean.com

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