FDA.reportPublic FDA data

Hand Sanitizer

Manufacturer
Partnership Marketing Limited | Evergreen Innovations LLC
Effective date
2020-08-03
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:23:36

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Dosage and administration

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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v. Purpose: Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

WARNINGS SECTION

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

Do not use

OTC - DO NOT USE SECTION

  • 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.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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.

Other information

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerin, hydrogen peroxide, purified water USP

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CANVIVA 2 fl oz (59 mL) Ginger and Lemongrass Back 3CANVIVA 2 fl oz (59 mL) Ginger and Lemongrass Back 3CANVIVA 2 fl oz (59 mL) Ginger and Lemongrass Back 2CANVIVA 2 fl oz (59 mL) Ginger and Lemongrass Back 2CANVIVA 2 FL OZ (59mL) Ginger and Lemongrass Back 1CANVIVA 2 FL OZ (59mL) Ginger and Lemongrass Back 1CANVIVA 2 fl oz (59 mL) Ginger and Lemongrass FrontCANVIVA 2 fl oz (59 mL) Ginger and Lemongrass FrontCANVIVA .5 Gal (64 fl oz) 1.89 L Back Label SF1 200CANVIVA .5 Gal (64 fl oz) 1.89 L Back Label SF1 200CANVIVA .5 Gal (64 fl oz) 1.89 L Back Label EZ1 200CANVIVA .5 Gal (64 fl oz) 1.89 L Back Label EZ1 200CANVIVA .5 Gal (64 fl oz) 1.89 L Front LabelCANVIVA .5 Gal (64 fl oz) 1.89 L Front Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
582753ethanol 70 % Topical SolutionPSN4
582753ethanol 0.7 ML/ML Topical SolutionSCD4
582753ethanol 70 % Topical SolutionSY4
582753ethyl alcohol 70 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78729-103-812023-01-30C16284748780-1f386c64a-175f-0266-e053-dadaa90a7c1aa7962f91-b0d2-1c92-e053-2a95a90ab089
78729-104-852023-01-30C16284748780-1f386c64a-175f-0266-e053-dadaa90a7c1aa7962f91-b0d2-1c92-e053-2a95a90ab089
78729-104-862023-01-30C16284748780-1f386c64a-175f-0266-e053-dadaa90a7c1aa7962f91-b0d2-1c92-e053-2a95a90ab089

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78729-103-81Hand Sanitizer70 mL in 1 BOTTLE, PUMPLIQUID704
78729-104-85Hand Sanitizer70 mL in 1 BOTTLE, PUMPLIQUID704
78729-104-86Hand Sanitizer59 mL in 1 BOTTLE, PLASTICLIQUID594

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78729-103HAND SANITIZER (ALCOHOL) LIQUID [PARTNERSHIP MARKETING LIMITED]4Legacy NDC, 1 package rows20200804_a7962f91-b0d2-1c92-e053-2a95a90ab089.zip
78729-104HAND SANITIZER (ALCOHOL) LIQUID [PARTNERSHIP MARKETING LIMITED]4Legacy NDC, 2 package rows20200804_a7962f91-b0d2-1c92-e053-2a95a90ab089.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78729-10378729-103-81
78729-10478729-104-85, 78729-104-86

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Name, UNII, Kind table
NameUNIIKind
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ETHYL PALMATEPY7890FR5MIACT
GINGER OILSAS9Z1SVUKIACT
JOJOBA OIL724GKU717MIACT
RAPIDGEL EZ133JH4A7R2KIACT
EAST INDIAN LEMONGRASS OILUP0M8M3VZWIACT
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ETHYL PALMATEPY7890FR5MIACT
GINGER OILSAS9Z1SVUKIACT
JOJOBA OIL724GKU717MIACT
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW)JZ1374NL9EIACT
AMINOMETHYLPROPANOLLU49E6626QIACT

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
abfdff65-93b4-594e-e053-2a95a90a13eba7962f91-b0d2-1c92-e053-2a95a90ab0892020-08-03WarningsExact identifier
spl id: abfdff65-93b4-594e-e053-2a95a90a13eb
spl set id: a7962f91-b0d2-1c92-e053-2a95a90ab089

Reported adverse events (FAERS/openFDA)#

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