Soldanizer
FDA Label NDC 77015-100

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by 3vets Llc for the product Soldanizer (NDC 77015-100). 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, 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 0.13%

Purpose

ANTIMICROBIAL

Uses

  • HAND SANITIZER HELPS REDUCE BACTERIA ON THE SKIN.
  • CAN BE USED REPEATEDLY.

Warnings

FOR EXTERNAL USE ONLY.

AVOID CONTACT WITH OR NEAR EYES WHEN USING THIS PRODUCT. IN CASE OF CONTACT, RINSE EYES THOROUGHLY WITH WATER.

IF IRRITATION OR RASH APPEARS, OR IF CONDITION PERSISTS, STOP USE AND CONTACT A DOCTOR.

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

  • SPRAY PRODUCT INTO THE PALM OF HAND.
  • RUB HANDS TOGETHER THOROUGHLY UNTIL DRY.
  • SUPERVISE CHILDREN UNDER 6 YEARS OF AGE WHEN USING PRODUCT.

Inactive Ingredients

WATER, DIDECYL DIMETHYL AMMONIUM CHLORIDE, PROPYLENE GLYCOL, METHYLPARABEN, DIAZOLIDINYL UREA, PROPYLPARABEN, COCAMIDOPROPYLAMINE OXIDE, ALLANTOIN, COCAMIDOPROPYL BETAINE, CETRIMONIUM CHLORIDE, TRIETHANOLAMINE, CITRIC ACID.

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