Hdx Gel
FDA Label NDC 63148-100

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Apollo Health And Beauty Care for the product Hdx (NDC 63148-100). 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 ingredients, purpose, uses, warnings, when using this product, do not use, stop use and ask a doctor, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredients

Ethyl Alcohol (70%)

Purpose

Antiseptic

Uses

To help reduce bacteria that can potentially cause disease. For use when soap and water are not available. 

Warnings

  • For External use only
  • Flammable
  • Keep away from source of heat or fire. 

When Using This Product

Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not Inhale.

Do Not Use

  • on children less than 2 months of age
  • on open skin wounds
  • on broken or damaged skin

Stop Use And Ask A Doctor

If Irritation or redness develops and lasts.

Keep Out Of Reach Of Children.

In case of accidental ingestion, get medical help or contact a Poison Control Center immediately

Directions

  • For occasional and personal use
  • Rub thoroughly into hands for at least 30 seconds. Allow to dry
  • Children under 6 years should be supervised when using this product

Other Information

  • Store at a temperature below 1100F (430C)
  • May discolor certain fabrics or surfaces

Inactive Ingredients

Water (Aqua), PEG-6, AMP-Acrylates/Vinyl Isodecanate Crosspolymer, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Glycerin, Isopropyl Alcohol, Tocopheryl Acetate, Ethylene Brasslate.

Questions Or Comments?

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