Sanix Alcohol Hand Rub

Manufacturer
Topiderm, Inc | Topiderm, Inc.
Effective date
2020-03-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 00:03:03

Label at a glance#

ProductSanix Alcohol Hand Rub
Active ingredientALCOHOL
Label structure8 sections

Indications and uses

Hand sanitizer for reduction of bacteria on the skin.

Dosage and administration

Apply enough product into the palm and rub hands together to thoroughly wet them Continue until the product dries without wiping off Supervise children when they are using the product Store below 110°F (43°C) May discolor some types of fabrics & surfaces.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62% (v/v)

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

Hand sanitizer for reduction of bacteria on the skin.

Warnings

WARNINGS SECTION

For external use only.

SPL UNCLASSIFIED SECTION

Flammable. Keep away from fire and flame.

SPL UNCLASSIFIED SECTION

Keep out of and away from the eyes. In case of eye contact flush thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. Not for use on infants.

If product is swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply enough product into the palm and rub hands together to thoroughly wet them

  • Continue until the product dries without wiping off
  • Supervise children when they are using the product
  • Store below 110°F (43°C)
  • May discolor some types of fabrics & surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Aloe Barbadensis Leaf Juice, Glycerin, Tocopheryl Acetate, Polysorbate 20, Isopropyl Alcohol, Isopropyl Palmitate, Tetrahydroxypropyl Ethylenediamine, Carbomer, Fragrance.

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTIBACTERIAL
Hand Sanitizer Gel
by REPLENIX®

Kills 99.9% of Most Illness Causing Germs*
Triple Action Moisturizers
Softens Hands with Aloe, Vitamin E & Glycerin

Made in USA
Trusted By
MEDICAL
PROFESSIONALS
Manufactured by Topix Pharmaceuticals

Net 8 fl.oz. (237ml)

PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label
PRINCIPAL DISPLAY PANEL - 237 ml Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581660ethanol 62 % Topical GelPSN2
581660ethanol 0.62 ML/ML Topical GelSCD2
581660ethanol 62 % Topical GelSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51326-900-08Sanix Alcohol Hand Rub240 mL in 1 BOTTLELIQUID2402

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51326-900SANIX ALCOHOL HAND RUB (ALCOHOL) LIQUID [TOPIDERM, INC]2Current NDC, Legacy NDC, 1 package rows20231201_a4fbb714-4f20-400a-ab98-f1c8807ce6fc.zip

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51326-90051326-900-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
Sanix Alcohol Hand RubALCOHOLTopiderm, Inca4fbb714-4f20-400a-ab98-f1c8807ce6fc2020-03-24WarningsExact identifier
ndc (package): 51326-900-08
ndc (product): 51326-900
ndc11 (package): 51326090008
spl id: 2af17da6-253d-4958-92ce-2dc70987b669
spl set id: a4fbb714-4f20-400a-ab98-f1c8807ce6fc

Reported adverse events (FAERS/openFDA)#

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