HANNA LABS INSTANT HAND SANITIZER

Manufacturer
MICRO CONNECTION ENTERPRISES INC
Effective date
2021-11-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:26:49

Label at a glance#

ProductHANNA LABS INSTANT HAND SANITIZER 70 PERCENT
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

Place quantity desired on the palm of one hand and rub together with the other. Children under 6 should be helped and supervised.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70% V/V

PURPOSE

OTC - PURPOSE SECTION

ANTIMICROBIAL

USE

INDICATIONS & USAGE SECTION

Hand Sanitizer helps reduce bacteria on skin contact, helps to avoid the spread of illness.

WARNINGS

WARNINGS SECTION

For external use only

Flammable. Keep away from fire or flame.

When using this product avoid contact with eyes. If contact occurs rinse with plenty of water. Do not ingest.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Store in a cool dry place. Poison Control Center 1-800-222-1222.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • Place quantity desired on the palm of one hand and rub together with the other.
  • Children under 6 should be helped and supervised.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aminomethyl Propanol, Glycerin, Fragrance, Water (Aqua)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hanna_Hand Sani Gel 70pct EtOH_1.7oz01b LBL_Hanna_Hand Sani Gel 70pct EtOH_1.7oz

01b LBL_Hanna_Hand Sani Gel 70pct EtOH_8oz01b LBL_Hanna_Hand Sani Gel 70pct EtOH_8oz

FDA-Initiated Inactive NDC Indexing#

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
76038-40276038-402-08, 76038-402-02

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
d103a715-883f-5671-e053-2995a90a7fda195de38e-babb-4128-a4f6-aba3058b2b1b2021-11-17WarningsExact identifier
spl id: d103a715-883f-5671-e053-2995a90a7fda
spl set id: 195de38e-babb-4128-a4f6-aba3058b2b1b

Reported adverse events (FAERS/openFDA)#

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