Genuine First Aid Pain Relieving Cream
FDA Label NDC 50814-079

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Gfa Production (xiamen) Co., Ltd. for the product Genuine First Aid Pain Relieving Cream (NDC 50814-079). 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 drug facts, active ingredients, purpose, uses, warnings, do not use, keep out of the reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts

Active Ingredients

Benzalkonium Chloride 0.13%

Lidocaine HCl 0.5%

Purpose

First Aid Antiseptic

Topical Analgesic

Uses

  • Temporary relief of pain associated with minor cuts, scrapes, and burns.
  • Helps pretect against harmful bacteria.

Warnings

For external use only.

Do Not Use

• in eyes • in large quantities • over raw or blistered areas, or on deep puncture wounds, animal bites, or serious burns • for more than one week unless directed by a doctor

Keep Out Of The Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center directly.

Directions

  • clean affected area
  • apply small amount not more than 3 times daily
  • may be covered with a sterile bandage

Other Information

  • store in a cool dry area 15° to 25° C (59° to 79°F)
  • tamper evident sealed packets
  • do not use any opened or torn packets

Inactive Ingredients

Aloe barbadensis leaf juice, Cetearyl alcohol, Disodium EDTA, Ethylhexylglycerin, Glycerin, Glyceryl stearate/PEG-100 stearate, Maltodextrin, Mineral oil, Phenoxyethanol, Propylene glycol, Purified water, Stearic acid, Triethanolamine.

Package Labeling:

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