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Manufacturer
Momar Inc. | ABC Compounding Co., Inc. | ABC Compounding Company of Texas, Inc.
Effective date
2018-05-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:58:54

Label at a glance#

ProductRedeem
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

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

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredients Section

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Drug Facts Box OTC-Purpose Section

OTC - PURPOSE SECTION

Antiseptic

Drug Facts Box OTC-Indications and 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

press valve once to deliver one squirt (about a quarter size) of foaming product onto the palm of your hand

rub hands together and allow to dry without wiping

Drug Facts Box OTC-Inactive Ingredients Section

INACTIVE INGREDIENT SECTION

water, DEA-C8-18 perfluoroalkylethyl phosphate, cetearyl alcohol, polysorbate 65, polysorbate 65, stearth-20, dimethicone PEG-8 meadowfoamate, meadowfoamamidopropyl betaine, PEG 40 hydrogenated castor oil, butane, propane

Redeem 4774 199g

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

product labelproduct label

477407P610.jpgRedeem 4774

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63533-77463533-774-25, 63533-774-26

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPANET75W9911L6IACT
BUTANE6LV4FOR43RIACT
WATER059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
Polysorbate 60CAL22UVI4MIACT
POLYOXYL 40 HYDROGENATED CASTOR OIL7YC686GQ8FIACT
MEADOWFOAMAMIDOPROPYL BETAINEHNV0L650LGIACT
Steareth-20L0Q8IK9E08IACT
DIETHANOLAMINE BIS(C8-C18 PERFLUOROALKYLETHYL)PHOSPHATE4J55VM509SIACT
POLYSORBATE 6514BGY2Y3MJIACT
DIMETHICONE PEG-8 SUCCINATEN39RWY20SEIACT
ALCOHOL3K9958V90MACTIB

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c5874e5b-c35e-993c-e053-2995a90a941109ae0a54-a1c8-421b-8da2-d4aa866079362021-06-24WarningsExact identifier
spl set id: 09ae0a54-a1c8-421b-8da2-d4aa86607936

Reported adverse events (FAERS/openFDA)#

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