FDA.reportPublic FDA data

Hada Hand Sanitizer

Manufacturer
Hada International S.A.
Effective date
2020-05-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:30:44

Label at a glance#

ProductHada Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Storage and handling

Other information Store between 15-30°C (59-86°F) Avoid freezing and excessive heat above 40°C (104°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 75% v/v

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Use

To help reduce bacteria on skin that can potentially cause disease

WARNINGS SECTION

Warnings
For external use only.
Flammable. Keep away from fire or flame.

OTC - WHEN USING SECTION

When using this product keep away from eyes. In case of eye contact, rinse eyes with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.

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 immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • Apply liberally to hands to cover all surfaces.
  • Rub hands together until dry.
  • Supervise children under 6 years old.
  • Not recommended for infants.

STORAGE AND HANDLING SECTION

Other information

  • Store between 15-30°C (59-86°F)
  • Avoid freezing and excessive heat above 40°C (104°F)

INACTIVE INGREDIENT SECTION

Inactive ingredients

Carbomer, glycerin, propylene glycol, triethanolamine, water

SPL UNCLASSIFIED SECTION

Manufactured for:

Hada International S.A. Zona Franca La Cayena KM8 LT7

MZ8, Barranquilla, Columbia

Calls: USA: (786) 447-8744

Made in Mexico

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

HAND SANITIZER 75%

Antiseptic Alcohol

NON-STERILE / TOPICAL SOLUTION

Kills 99.9% of most common germs

Hada® +

4.2 Qts (4 L)

Alcohol antiseptic FinalAlcohol antiseptic Final

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42377-01442377-014-40

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
PROPYLENE GLYCOL6DC9Q167V3IACT
TROLAMINE9O3K93S3TKIACT
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE0A5MM307FCIACT

Source Document#

Source XML · Source PDF

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
c5601431-bdc4-e982-e053-2995a90a3068a589d473-f0a3-5745-e053-2995a90a5cee2021-06-22WarningsExact identifier
spl set id: a589d473-f0a3-5745-e053-2995a90a5cee

Reported adverse events (FAERS/openFDA)#

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