Recens Foam

Manufacturer: Certus Medical, Inc. | ABC Compounding Co., Inc.
Effective date: 2025-11-20
Label type: HUMAN OTC DRUG LABEL
Version: 4
Source: full-release
Hydrated at: 2026-06-01 01:17:28

Label at a glance#

ProductRecens Foam

Active ingredientALCOHOL

Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70% v/v

Drug Facts Box OTC-Purpose Section

OTC - PURPOSE SECTION

Antiseptic

Drug Facts Box OTC-Indications & Usage Section

INDICATIONS & USAGE SECTION

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

Drug Facts Box OTC-Warnings Section

WARNINGS SECTION

FLAMMABLE, keep away from fire and flames

For external use only

Drug Facts Box OTC-When Using Section

OTC - WHEN USING SECTION

do not get into eyes

if contact occurs, rinse eyes thoroughly with water

Drug Facts Box OTC-Stop Use Section

OTC - STOP USE SECTION

irritation and redness develop

Drug Facts Box OTC-Keep Out of Reach of Children Section

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

DOSAGE & ADMINISTRATION SECTION

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

Drug Facts Box OTC-Inactive Ingredient Section

INACTIVE INGREDIENT SECTION

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

Recens Foam 6968

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionRecens Foam 6968

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
616805	ethanol 70 % Topical Foam	PSN	4
616805	ethanol 0.7 ML/ML Topical Foam	SCD	4
616805	ethanol 70 % Topical Foam	SY	4

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
75990-968-07	Recens Foam	700 mL in 1 BAG	LIQUID	700	4
75990-968-12	Recens Foam	1000 mL in 1 BAG	LIQUID	1000	4
75990-968-17	Recens Foam	532 mL in 1 BOTTLE, PLASTIC	LIQUID	532	4

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 5 matching rows.

Recens Foam
ALCOHOL
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER
WATER
PROPYLENE GLYCOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
75990-968	75990-968-07, 75990-968-12, 75990-968-17

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMER	D76Z87928N	IACT
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
PROPYLENE GLYCOL	6DC9Q167V3	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Recens Foam	ALCOHOL	Certus Medical, Inc.	ea384dfc-c894-3124-e053-2a95a90a81c2	2025-11-20	Warnings	Exact identifier ndc (package): 75990-968-07 ndc (package): 75990-968-17 ndc (package): 75990-968-12 ndc (product): 75990-968 ndc11 (package): 75990096812 ndc11 (package): 75990096817 ndc11 (package): 75990096807 spl id: 440c3f5a-1bc5-257c-e063-6394a90af204 spl set id: ea384dfc-c894-3124-e053-2a95a90a81c2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.