FDA.reportPublic FDA data

Sanative Gel Hand Sanitizer 70 Alcohol Antiseptic

Manufacturer
Heretic Spirits
Effective date
2020-08-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:16:38

Label at a glance#

ProductSanative Gel Hand Sanitizer 70 Alcohol Antiseptic
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

Hand sanitizer to help reduce bacteria on the skin that could cause disease. For use when soap and water are not available. Recommended for repeated use.

Dosage and administration

Rub thoroughly into hands for at least 30 seconds. Allow to dry. Supervise children when they use this product. For occasional and personal domestic use.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol (Ethanol, Ethanol) 70 % (v/v)

PURPOSE

OTC - PURPOSE SECTION

Antiseptic

USES

INDICATIONS & USAGE SECTION

Hand sanitizer to help reduce bacteria on the skin that could cause disease. For use when soap and water are not available. Recommended for repeated use.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Rub thoroughly into hands for at least 30 seconds. Allow to dry. Supervise children when they use this product. For occasional and personal domestic use.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Purified water, acrylates copolymer, triethanolamine, denatonium benzoate, hydrogen peroxide. This product does not contain mercury.

WARNINGS:

WARNINGS SECTION

Flammable. Keep away from heat or flame. For external use only.

Do not use

OTC - DO NOT USE SECTION

on children/infants less than 2 years of age (unless directed by a doctor/ physician/ health care practitioner/ health care provider/ health care professional).

When using the product

OTC - WHEN USING SECTION

do no use in or near the eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Stop use and ask doctor

OTC - STOP USE SECTION

if irratition or rash occurs. These may be signs of a serious condition.

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.

Package Labeling:236ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

236mL236mL

Package Labeling:3790ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

3790 mL3790 mL

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
80317-00180317-001-01, 80317-001-02

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
WATER059QF0KO0RIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
TROLAMINE9O3K93S3TKIACT
DENATONIUM BENZOATE4YK5Z54AT2IACT
HYDROGEN PEROXIDEBBX060AN9VIACT
ALCOHOL3K9958V90MACTIB

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
d22ddafa-b75e-4cae-e053-2a95a90a31f1ae2e006c-035e-6c35-e053-2a95a90ab7b12021-12-02WarningsExact identifier
spl set id: ae2e006c-035e-6c35-e053-2a95a90ab7b1

Reported adverse events (FAERS/openFDA)#

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