Be Gone Scratch-n-itch
FDA Label NDC 68428-727

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Washington Homeopathic Products for the product Be Gone Scratch-n-itch (NDC 68428-727). 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 ingredients, uses, keep out of reach of children, indications, stop use and ask doctor, directions, inactive ingredients, principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredients

GRINDELIA    ø

CAMPHOR    ø

Uses

To relieve itchy skin.

Keep Out Of Reach Of Children

Keep out of reach of children.

Indications

Indications:

GRINDELIA   Rash

CAMPHOR    Coldness

Stop Use And Ask Doctor

For external use only. If symptoms persist/worsen or if pregnant/nursing, consult your practitioner. Do not use if seal with WHP logo is broken or missing.

Directions

Adults: Apply locally several times daily or as needed.

Inactive Ingredients

20% Ethyl alcohol

USP water

Principal Display Panel

Be gone SCRATCH-N-ITCH Label

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