FDA.reportPublic FDA data

Fast

Manufacturer
ABC Compounding Co., Inc.
Effective date
2025-11-19
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 01:17:12

Label at a glance#

ProductFast
Active ingredientALCOHOL
Label structure10 sections

Label contents#

Full prescribing information#

Drug Facts Box OTC-Active Ingredient Section

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 70%

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

press pump twice to deliver two squirts (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 Ingredient Section

INACTIVE INGREDIENT SECTION

water, peg 10 acrylate/perfluorohexylethyl acrylate copolymer, perfluorohexylethyl alcohol, propylene glycol

Fast

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FastFast

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
616805ethanol 70 % Topical FoamPSN6
616805ethanol 0.7 ML/ML Topical FoamSCD6
616805ethanol 70 % Topical FoamSY6

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62257-658-08Fast1 in 1 BOXLIQUID16
62257-658-08Fast1000 mL in 1 BAGLIQUID10006
62257-658-10Fast1000 mL in 1 CARTRIDGELIQUID10006
62257-658-11Fast1000 mL in 1 BOTTLE, PLASTICLIQUID10006
62257-658-12Fast1000 mL in 1 BAGLIQUID10006
62257-658-14Fast3785 mL in 1 BOTTLE, PLASTICLIQUID37856
62257-658-17Fast532 mL in 1 BOTTLE, PLASTICLIQUID5326
62257-658-18Fast50 mL in 1 BOTTLE, PLASTICLIQUID506

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62257-65862257-658-17, 62257-658-10, 62257-658-11, 62257-658-12, 62257-658-08, 62257-658-18, 62257-658-14

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
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-10 ACRYLATE/PERFLUOROHEXYLETHYL ACRYLATE COPOLYMERD76Z87928NIACT
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
FastALCOHOLABC Compounding Co., Inc.4f958247-5370-4250-b2eb-39faa97199392025-11-19WarningsExact identifier
ndc (package): 62257-658-10
ndc (package): 62257-658-08
ndc (package): 62257-658-17
ndc (package): 62257-658-14
ndc (package): 62257-658-11
ndc (package): 62257-658-18
ndc (package): 62257-658-12
ndc (product): 62257-658
ndc11 (package): 62257065811
ndc11 (package): 62257065818
ndc11 (package): 62257065808
ndc11 (package): 62257065810
ndc11 (package): 62257065817
ndc11 (package): 62257065814
ndc11 (package): 62257065812
spl id: 43f5d499-05e7-5411-e063-6294a90a2a57
spl set id: 4f958247-5370-4250-b2eb-39faa9719939

Reported adverse events (FAERS/openFDA)#

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