ISOPROPYL Alcohol Wipes

Manufacturer
Reynard (Ningbo) Biotechnology Co., Ltd.
Effective date
2022-04-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:49:18

Label at a glance#

ProductISOPROPYL Alcohol Wipes
Active ingredientBENZALKONIUM CHLORIDE, ISOPROPYL ALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Store in a cool and dry place

INACTIVE INGREDIENT SECTION

Purified Water, non-woven cloth, Aloe Extract, Glycerin

INDICATIONS & USAGE SECTION

●For occasional and domestic use only.
●Use a single wipe at a time.
●Rub thoroughly into hands for 30 seconds and allow to dry.
●Discard soiled wipe in trash.
●DO not flush into toilet.
●Keep lid and flap closed to prevent drying.
●Supervise children when using this product.

OTC - ACTIVE INGREDIENT SECTION

Isopropyl alcohol

Benzalkonium Chloride

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of children

OTC - PURPOSE SECTION

Disinfection
Sterilization
No Rinseing

WARNINGS SECTION

For external use only.
●Flammable, keep away from fire or flame Ask a doctor before use if you have
●deep or puncture wounds, bites or serious burns When using this product
●do not get into eyes
●do not apply over large areas of body
●do not use for prolonged periods of time unless directed by doctor

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55485-005-01ISOPROPYL Alcohol Wipes50 in 1 PACKETCLOTH502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55485-005ISOPROPYL ALCOHOL WIPES CLOTH [REYNARD (NINGBO) BIOTECHNOLOGY CO., LTD.]2Legacy NDC, 1 package rows20220422_a92ffff2-5b03-2dd4-e053-2a95a90af969.zip

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55485-00555485-005-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
dd21d31d-d3d3-43b7-e053-2995a90a93d3a92ffff2-5b03-2dd4-e053-2a95a90af9692022-04-20WarningsExact identifier
spl id: dd21d31d-d3d3-43b7-e053-2995a90a93d3
spl set id: a92ffff2-5b03-2dd4-e053-2a95a90af969

Reported adverse events (FAERS/openFDA)#

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