Elf Zit Zapper
FDA Label NDC 52664-007

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hangzhou Facecare Cosmetics Co., Ltd. for the product Elf Zit Zapper (NDC 52664-007). 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, otc - purpose, indications & usage, warnings, otc - when using, otc - ask doctor, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Active Ingredient

Active Ingredient:

Salicylic Acid 1.0%

Otc - Purpose

Purpose:

Acne

Indications & Usage

Uses:

  • Zap zits away with the unique blend of Salicylic Acid, Tea Tree, Witch Hazel, and Camphor
  • The special clear formula helps to fight and prevent  acne,  reduce redness and swelling,  minimize pore size and clear skin

Warnings

Warning:

For external use only

Otc - When Using

When Using This Product:

Do not get into eyes

Avoid using on wounds or on areas of eczema

Otc - Ask Doctor

Stop Use and Ask A Doctor If:

Rash or irritation develops and lasts

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

Dosage & Administration

Directions:

Apply directly to blemishes nightly

Storage And Handling

Other Information:

Store at room temperature 20-25C (68-77F)

Inactive Ingredient

Inactive Ingredient:

Water, Witch Hazel (Hamamelis Virginiana) Distillate, Alcohol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Polyacrylamide, C13-14 Isoparaffin, Laureth-7, Cinnamomum Camphora (Camphor) Bark Oil

Package Label.Principal Display Panel

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Label (Zit)

Label (Zit)

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