Sanell Hand Sanitizer

Manufacturer: OraLabs
Effective date: 2025-04-28
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-06-01 00:59:52

Label at a glance#

ProductSanell Hand Sanitizer

Active ingredientALCOHOL

Label structure8 sections

Indications and uses

For handwashing to decrease bacteria on the skin.

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. Supervise children in the use of this product.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 63.00%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Keep Out of Reach of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed get medical help or contact a Poison Control Center right away.

Uses

INDICATIONS & USAGE SECTION

For handwashing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only: Hands. Flammable. Keep away from fire or flame. Do not use in the eyes. In case of contact, rinse eyes thoroughly with water.. Stop use and ask a doctor: if irritation and redness develop and persists for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

Wet hands thoroughly with product and allow to dry without wiping. Supervise children in the use of this product.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Dimethicone, Disodium EDTA, DMDM Hydantoin, Fragrance, Polysorbate 20, Propanediol, Water.

Package/Label Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
63645-177-01	2025-04-28	C162847	48780-1	2cef2736-ab18-d83d-e063-dadaa90ab31f	Drug Facts
63645-177-01	2025-01-30	C162847	48780-1	2cef2736-ab18-d83d-e063-dadaa90ab31f	Drug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
63645-177-01	Sanell Hand Sanitizer	7.5 mL in 1 BOTTLE	SPRAY	7.5		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
63645-177	SANELL HAND SANITIZER (ALCOHOL) SPRAY [ORALABS]	3	Current NDC, Legacy NDC, 1 package rows	20250429_7184b9ad-0125-413d-b054-f46239b8ca92.zip

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

Sanell Hand Sanitizer
Alcohol
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
63645-177	63645-177-01

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
Name	UNII	Kind
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
Sanell Hand Sanitizer	ALCOHOL	OraLabs	7184b9ad-0125-413d-b054-f46239b8ca92	2025-04-28	Warnings	Exact identifier ndc (package): 63645-177-01 ndc (product): 63645-177 ndc11 (package): 63645017701 spl id: 33dd465c-2d73-d1d6-e063-6294a90a8f3f spl set id: 7184b9ad-0125-413d-b054-f46239b8ca92

Reported adverse events (FAERS/openFDA)#

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