Zuum 70 Ethyl Alcohol Antispetic Hand Sanitizer

Manufacturer
U.S. Cotton Mexico, S. de R.L. de C.V.
Effective date
2020-11-24
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:05:47

Label at a glance#

ProductZuum 70 Ethyl Alcohol Antispetic Hand Sanitizer
Active ingredientALCOHOL
Label structure8 sections

Dosage and administration

wet hands thoroughly with product and allow to dry without wiping

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use

INDICATIONS & USAGE SECTION

For hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

Flammable, keep away from fire or flame

Do not use

OTC - DO NOT USE SECTION

in the eyes

Stop use and ask a doctor

OTC - STOP USE SECTION

  • irritation and redness develop
  • condition persists for more than 72 hours

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.

Directions

DOSAGE & ADMINISTRATION SECTION

wet hands thoroughly with product and allow to dry without wiping

Other information

SPL UNCLASSIFIED SECTION

Do not leave open

Inactive ingredients

INACTIVE INGREDIENT SECTION

Denatonium benzoate, water

Questions?

OTC - QUESTIONS SECTION

505-962-3014

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
77388-000-012022-01-28C16284748780-1d6a99b39-7fff-a426-e053-dadaa90af4c2Zuum 70% Ethyl Alcohol Antispetic Hand Sanitizer

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
77388-000ZUUM 70 ETHYL ALCOHOL ANTISPETIC HAND SANITIZER (ALCOHOL) SOLUTION [U.S. COTTON MEXICO, S. DE R.L. DE C.V.]2Legacy NDC20201125_aa5844de-9ef4-092e-e053-2995a90a315a.zip

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
77388-00077388-000-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
DENATONIUM BENZOATE4YK5Z54AT2IACT
WATER059QF0KO0RIACT
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
b4de6d37-61f8-e4cc-e053-2a95a90a4757aa5844de-9ef4-092e-e053-2995a90a315a2020-11-24WarningsExact identifier
spl id: b4de6d37-61f8-e4cc-e053-2a95a90a4757
spl set id: aa5844de-9ef4-092e-e053-2995a90a315a

Reported adverse events (FAERS/openFDA)#

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