FDA.reportPublic FDA data

Hand Sanitizer wipes

Manufacturer
Newrain International Llc
Effective date
2020-07-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:21:16

Label at a glance#

ProductHand Sanitizer wipes
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Clean the affected area Apply product on the affected area 1 to 3 times a day After application, the area may be covered with a sterile bandage, if bandaging, let area dry first.

Storage and handling

Do not apply internally. Keep package closed. Hold away from face when opening Store below 110F

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%. Purpose: First Aid Antiseptic

Purpose

OTC - PURPOSE SECTION

First Aid Antiseptic, Hand Sanitizer wipes

Use

INDICATIONS & USAGE SECTION

Use first aid wipes to help prevent the risk of infection of minor: cuts, scrapes, and burns.

Warnings

WARNINGS SECTION

For external use only

Flammable keep away from open flames, heat, or sparks.

When using this product

OTC - WHEN USING SECTION

  • do not get in eyes
  • do not apply over large area of the body
  • do not use longer than 1 week unless directed by a doctor

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 our of reach of children. If swallowed, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Clean the affected area
  • Apply product on the affected area 1 to 3 times a day
  • After application, the area may be covered with a sterile bandage, if bandaging, let area dry first.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified water

Other information

STORAGE AND HANDLING SECTION

  • Do not apply internally.
  • Keep package closed.
  • Hold away from face when opening
  • Store below 110F

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

80 PCS 76931-001-01

PDPPDP

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
79693-00179693-001-01
78150-003

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
WATER059QF0KO0RIACT
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
aaed1bcc-6571-5fb2-e053-2995a90aa18aaa9eff1c-822d-129f-e053-2995a90a97262020-07-21WarningsExact identifier
spl set id: aa9eff1c-822d-129f-e053-2995a90a9726

Reported adverse events (FAERS/openFDA)#

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