FDA.reportPublic FDA data

FA Alcohol swab

Manufacturer
HLB CO.,LTD_Healthcare
Effective date
2023-12-07
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
legacy-cache
Hydrated at
2026-08-01 21:18:43

Label at a glance#

ProductFA Alcohol swab
Active ingredientIsopropyl Alcohol
Label structure9 sections

Indications and uses

■ Used to help reduce germ and bacteria that potentially can cause disease.

Dosage and administration

■ After take away one pad, wiped injection or disinfection site smoothly.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Water

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

WARNINGS

WARNINGS SECTION

For external use only. Flammable. Keep away from heat or flame

--------------------------------------------------------------------------------------------------------
When using this product ■ do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water ■ avoid contact with broken skin ■ do not inhale or ingest
--------------------------------------------------------------------------------------------------------
Stop use and ask a doctor if irritation or rash appears and lasts

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Uses

INDICATIONS & USAGE SECTION

■ Used to help reduce germ and bacteria that potentially can cause disease.

Directions

DOSAGE & ADMINISTRATION SECTION

■ After take away one pad, wiped injection or disinfection site smoothly.

Other Information

OTHER SAFETY INFORMATION

■ Store below 86℉(Between 1~30℃)

■ May discolor certain fabrics or surfaces

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of carton
Image of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74932-340-022024-01-30C16284748780-1f386c64a-37cd-0266-e053-dadaa90a7c1a4f65be2e-53ef-4b03-ba8e-79e4c67fda4d
74932-340-022023-12-12C16284748780-1f386c64a-37cd-0266-e053-dadaa90a7c1a4f65be2e-53ef-4b03-ba8e-79e4c67fda4d
74932-340-022023-01-30C16284748780-1f386c64a-37cd-0266-e053-dadaa90a7c1a4f65be2e-53ef-4b03-ba8e-79e4c67fda4d

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74932-34074932-340-01, 74932-340-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
Isopropyl AlcoholND2M416302ACTIB
Water059QF0KO0RIACT

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
1bf03306-3634-8871-e063-6394a90a90444f65be2e-53ef-4b03-ba8e-79e4c67fda4d2024-06-28WarningsExact identifier
spl set id: 4f65be2e-53ef-4b03-ba8e-79e4c67fda4d

Reported adverse events (FAERS/openFDA)#

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