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 22:26:53

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.

Contacts and useful links#

PhonePoison Help1-800-222-1222

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

ETHYL ALCOHOL 70%

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

Glycerin, Water (Aqua), Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Hanna_Hand Sani Spray_5.9mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
76038-403-59	2023-01-30	C162847	48780-1	f386c649-b585-0266-e053-dadaa90a7c1a	THE MICRO CONNECTION - HANNA LABS INSTANT HAND SANITIZER (SPRAY) - 70% ETHYL ALCOHOL (76038-403)

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

HANNA LABS INSTANT HAND SANITIZER 70 PERCENT
ETHYL ALCOHOL
GLYCERIN
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
76038-403	76038-403-59

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
Name	UNII	Kind
GLYCERIN	PDC6A3C0OX	IACT
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
d103ac3e-c8de-4546-e053-2995a90aa0f5			66d9a498-a05a-45fd-9835-febf39d6b227	2021-11-17	Warnings	Exact identifier spl id: d103ac3e-c8de-4546-e053-2995a90aa0f5 spl set id: 66d9a498-a05a-45fd-9835-febf39d6b227

Reported adverse events (FAERS/openFDA)#

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