FDA.reportPublic FDA data

SaniMax

Manufacturer
SYNDICATE ONE GROUP INC
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:22:20

Label at a glance#

ProductSaniMax
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Wipe down surface thoroughly and allow to air-dry. For children under 6, use only under adult supervision Not recommended for infants

Storage and handling

do not store above 105°F

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 75% v/v.

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

decreases bacteria on skin.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat and flame.

When using the product

  • keep out of eyes, in case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not inhale or ingest
  • do not reuse wipe
  • do not flush in toilet

Stop use and ask a doctor if skin irritation develops.

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

  • Wipe down surface thoroughly and allow to air-dry.
  • For children under 6, use only under adult supervision
  • Not recommended for infants

Other information

STORAGE AND HANDLING SECTION

  • do not store above 105°F

Inactive ingredients

INACTIVE INGREDIENT SECTION

purified water, glycerin. aloe barbadensis extract, phenoxyethanol, ethylhexlyglycerin, propylene glycol

Product Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1307051ethanol 75 % Medicated PadPSN1
1307051ethanol 0.75 ML/ML Medicated PadSCD1
1307051ethanol 75 % Hand Sanitizer WipesSY1
1307051ethyl alcohol 75 % Topical ClothSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
79308-001-012022-01-28C16284748780-1d6a99b39-77dd-a426-e053-dadaa90af4c238bdc38a-c167-41b6-ba0d-8a114cbaf16d
79308-001-022022-01-28C16284748780-1d6a99b39-77dd-a426-e053-dadaa90af4c238bdc38a-c167-41b6-ba0d-8a114cbaf16d
79308-001-032022-01-28C16284748780-1d6a99b39-77dd-a426-e053-dadaa90af4c238bdc38a-c167-41b6-ba0d-8a114cbaf16d

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
79308-001-01SaniMax80 in 1 CANISTERCLOTH801
79308-001-01SaniMax4.3 mL in 1 NOT APPLICABLECLOTH4.31
79308-001-02SaniMax80 in 1 CANISTERCLOTH801
79308-001-02SaniMax4.3 mL in 1 NOT APPLICABLECLOTH4.31
79308-001-03SaniMax80 in 1 CANISTERCLOTH801
79308-001-03SaniMax4.3 mL in 1 NOT APPLICABLECLOTH4.31

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
79308-001SANIMAX (ALCOHOL) CLOTH [SYNDICATE ONE GROUP INC]1Legacy NDC, 6 package rows20200724_38bdc38a-c167-41b6-ba0d-8a114cbaf16d.zip

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
79308-00179308-001-01, 79308-001-02, 79308-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MACTIB
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
ALOE VERA LEAFZY81Z83H0XIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PROPYLENE GLYCOL6DC9Q167V3IACT

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
dc5b6a1f-23d3-4be7-b5ec-21c0bd845fe438bdc38a-c167-41b6-ba0d-8a114cbaf16d2020-06-26WarningsExact identifier
spl id: dc5b6a1f-23d3-4be7-b5ec-21c0bd845fe4
spl set id: 38bdc38a-c167-41b6-ba0d-8a114cbaf16d

Reported adverse events (FAERS/openFDA)#

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