Sundrops 75 Gel
FDA Label NDC 63621-356

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Sunburst Chemicals, Inc. for the product Sundrops 75 (NDC 63621-356). 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, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 60% v/v

Purpose

Skin Sanitizer

Use

To help reduce amount of bacteria on the skin

Warnings

Flammable. Keep away from fire or flame.

For external use only. If swallowed, seek medical attention.

Otc - When Using

When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact doctor immediately.

Otc - Stop Use

Stop use and consult a doctor when skin irritation appears and lasts.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Directions

  • Place 5 grams or palmful of product in one hand.
  • Spread on hands and rub into skin until dry.
  • Place a smaller amount (2.5 grams) in one hand & spread over hands & wrists.
  • Rub into skin until dry.
  • Supervise children while using this product.

Inactive Ingredients

Water, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine

Package Label.Principal Display Panel

SUNBURST CHEMICALS

SunDrops 75 - 8 fl. oz.

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