SC Health Instant Hand Sanitizer

Manufacturer
SC Health SPV, LLC
Effective date
2022-10-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:50:28

Label at a glance#

ProductSC Health Instant Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

wet hands thoroughly with product. allow to dry without wiping.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 75%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

for hand sanitizing to decrease bacteria on the skin.

Warnings

WARNINGS SECTION

Flammable,keep away from fire or flame

For external use only

Do not use

OTC - DO NOT USE SECTION

on damaged,inflamed,or broken skin.

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes.

in case of contact with eyes,rinse thoroughly with water.

Stop use and ask a doctor if

OTC - STOP USE SECTION

irritation or redness develops and lasts for more than 72 hours.

Keep out of reach of chilldren.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product.

allow to dry without wiping.

Inactive ingredients

INACTIVE INGREDIENT SECTION

acrylates/C 10-30 alkyl acrylate crosspolymer,aloe vera(aloe barbadensis)leaf extract,glycerin,triethanolamine,water.

Package Labeling: 20ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label1Label1

Package Labeling: 50ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label2Label2

Package Labeling: 100ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: 200ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling: 500ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

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
78633-00078633-000-01, 78633-000-02, 78633-000-03, 78633-000-04, 78633-000-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
d27c2b32-3c29-1e3d-e053-2995a90aca45a8c5db08-3491-3ee8-e053-2995a90ad97f2022-10-29WarningsExact identifier
spl id: d27c2b32-3c29-1e3d-e053-2995a90aca45
spl set id: a8c5db08-3491-3ee8-e053-2995a90ad97f

Reported adverse events (FAERS/openFDA)#

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