Sundrops 87 Soap
FDA Label NDC 63621-387

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 87 (NDC 63621-387). 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 - 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.

Label Section Quick Index

​Active Ingredient

Benzalkonium Chloride 0.1%

​Purpose

Skin Antimicrobial

Use

Reduces amount of bacteria on hands

​Warnings

For external use only.

When using this product avoid contact with eyes.  In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Otc - Keep Out Of Reach Of Children

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

​Directions

  • Pump a small amount of foam into palm of hand.
  • Scrub thoroughly for at least fifteen seconds.
  • Risne completely and dry.

​Inactive Ingredients

Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate, Fragrance

* Please review the disclaimer below.