Recens Foam Liquid
FDA Label NDC 75990-968

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Certus Medical, Inc. for the product Recens Foam (NDC 75990-968). 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 box otc-active ingredient section, drug facts box otc-purpose section, drug facts box otc-indications & usage section, drug facts box otc-warnings section, drug facts box otc-when using section, drug facts box otc-stop use section, drug facts box otc-keep out of reach of children section, drug facts box otc-dosage & administration section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Drug Facts Box Otc-Active Ingredient Section

Ethyl Alcohol 70% v/v

Drug Facts Box Otc-Purpose Section

Antiseptic

Drug Facts Box Otc-Indications & Usage Section

for hand-washing to decrease bacteria on the skin, only when water is not available

Drug Facts Box Otc-Warnings Section

FLAMMABLE, keep away from fire and flames

For external use only

Drug Facts Box Otc-When Using Section

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box Otc-Stop Use Section

irritation and redness develop

Drug Facts Box Otc-Keep Out Of Reach Of Children Section

if swallowed, get medical help or contact a Poison Control Center right away

Drug Facts Box Otc-Dosage & Administration Section

 apply to hands and rub lightly until dry without wiping or rinsing

Drug Facts Box Otc-Inactive Ingredient Section

water, PEG-10 acrylate, perfluorohexylethyl acrylate copolymer, propylene glycol

Recens Foam 6968

Image Description (6968m8pm)

Image Description (6968m8pm)

Recens Foam 6968

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