Manildra Stay Safe

Manufacturer
Manildra Milling Coporation
Effective date
2020-07-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-05-31 23:22:32

Label at a glance#

ProductManildra Stay Safe Alcohol Antiseptic 80% Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Alcohol 80% v/v

OTC - PURPOSE SECTION

Purpose
Antiseptic

INDICATIONS & USAGE SECTION

Uses

  • hand sanitizer to help reduce bacteria that potentially can cause disease
  • for use when soap and water are not available

WARNINGS SECTION

Warnings
For external use only.

Flammable. Keep away from heat or flame.

OTC - DO NOT USE SECTION

Do not use

  • in children less than 2 months of age
  • on open skin wounds

OTC - WHEN USING SECTION

When using this product keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions

  • place enough product on hands to cover all surfaces
  • rub hands together until dry
  • supervise children under 6 years of age when using this product to avoid swallowing

INACTIVE INGREDIENT SECTION

Inactive ingredients

glycerin, hydrogen peroxide, purified water USP

SPL UNCLASSIFIED SECTION

MANILDRA GROUP

100% AUSTRALIAN OWNED

Made in Australia

Distributed by: Manildra Milling Corporation
4501 College Blvd, Suite 310, Leawood, KS 66211

manildra.com.au • 1-800-323-8435

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

stay safe™
MANILDRA STAY SAFE™
ALCOHOL ANTISEPTIC 80%
TOPICAL SOLUTION HAND SANITIZER.

Non-Sterile Solution
FLAMMABLE LIQUID
5L (1.3 Gal)

Manildra Stay Safe FinalManildra Stay Safe Final

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1039339ethanol 80 % Topical SolutionPSN3
1039339ethanol 0.8 ML/ML Topical SolutionSCD3
1039339ethanol 80 % Topical SolutionSY3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79268-001-052021-07-23C16284748780-1c7ccaba7-14fd-fd44-e053-dadaa90aa01bManildra Stay Safe Alcohol 80% Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79268-001-05Manildra Stay SafeAlcohol Antiseptic 80% Hand Sanitizer5 L in 1 JUGLIQUID53

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79268-001MANILDRA STAY SAFE ALCOHOL ANTISEPTIC 80% HAND SANITIZER (ETHANOL) LIQUID [MANILDRA MILLING COPORATION]3Legacy NDC, 1 package rows20200725_aa1c5bcc-e97c-fecc-e053-2995a90abeca.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79268-00179268-001-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ab35cae4-c383-2bad-e053-2995a90a3700aa1c5bcc-e97c-fecc-e053-2995a90abeca2020-07-24WarningsExact identifier
spl id: ab35cae4-c383-2bad-e053-2995a90a3700
spl set id: aa1c5bcc-e97c-fecc-e053-2995a90abeca

Reported adverse events (FAERS/openFDA)#

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