FDA.reportPublic FDA data

First Aid Direct Antiseptic Wipe

Manufacturer
Cintas Corporation | Changzhou Maokang Medical Products Co., Ltd.
Effective date
2025-09-29
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 01:15:10

Label at a glance#

ProductFirst Aid Direct Antiseptic Wipe
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient (in each towelette)

Benzalkonium Chloride 0.133%

OTC - PURPOSE SECTION

Purpose

first aid antiseptic

INDICATIONS & USAGE SECTION

Uses

first aid to reduce bacteria in minor cuts, scrapes and burns

WARNINGS SECTION

Warnings

For external use only

OTC - DO NOT USE SECTION

Do not use

  • in the eyes or apply over large areas of the body
  • longer than 1 week unless directed by a doctor

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • deep or puncture wounds
  • animal bites
  • serious burns

OTC - STOP USE SECTION

Stop use and ask a doctor if

  • condition persists or gets worse

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

Directions

  • tear open packet, unfold, use and discard
  • clean the affected area
  • maybe covered with a sterile bandage. If bandaged, let dry first.

OTHER SAFETY INFORMATION

Other information

  • do not use if packet is torn, cut or opened
  • store at room temperature

INACTIVE INGREDIENT SECTION

Inactive ingredients

purified water, sodium bicarbonate

OTC - QUESTIONS SECTION

Questions? 1-877-973-2811

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Antiseptic Wipe

One Wipe Saturated with Benzalkonium Chloride

EXTERNAL USE ONLY

LabelLabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
42961-127-01First Aid Direct Antiseptic Wipe1.4 mL in 1 PACKETSPONGE1.45
42961-127-02First Aid Direct Antiseptic Wipe10 in 1 BAGSPONGE105
42961-127-03First Aid Direct Antiseptic Wipe100 in 1 BOXSPONGE1005

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
42961-12742961-127-01, 42961-127-02, 42961-127-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
SODIUM BICARBONATE8MDF5V39QOIACT
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
First Aid Direct Antiseptic WipeBENZALKONIUM CHLORIDECintas Corporationa23f3685-7213-4cc0-97b2-588fb12247922025-09-29WarningsExact identifier
ndc (package): 42961-127-03
ndc (package): 42961-127-01
ndc (package): 42961-127-02
ndc (product): 42961-127
ndc11 (package): 42961012703
ndc11 (package): 42961012701
ndc11 (package): 42961012702
spl id: d4120dd5-cf03-466f-b7fa-da23c47b1999
spl set id: a23f3685-7213-4cc0-97b2-588fb1224792

Reported adverse events (FAERS/openFDA)#

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