FDA.reportPublic FDA data

Zen Hand Sanitizer

Manufacturer
Zen Enterprises | Dr.Sankunnis Ayurvedic Research Foundation Pvt Ltd
Effective date
2020-08-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:18:05

Label at a glance#

ProductZen Hand Sanitizer
Active ingredientALCOHOL
Label structure11 sections

Dosage and administration

Place enough product on hands to cover your hands. Rub hands briskly until dry. No rinsing required No towels needed

Storage and handling

Do not store above 110F (43C) May discolor certain fabrics or surfaces

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v.

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

Hand Sanitizer to help reduce bacteria that potentially could cause disease. Recommended for repeated use

Warnings

WARNINGS SECTION

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

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, 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 right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Place enough product on hands to cover your hands. Rub hands briskly until dry.
  • No rinsing required
  • No towels needed

Other information

STORAGE AND HANDLING SECTION

  • Do not store above 110F (43C)
  • May discolor certain fabrics or surfaces

Inactive ingredients

INACTIVE INGREDIENT SECTION

Vitamin E, Demineralized Water, Glycerin

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label 1label 1labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73048-002-012024-01-30C16284748780-11030e365-2a23-111a-e063-dadaa90a10e2Zen Hand Sanitizer
73048-002-022024-01-30C16284748780-11030e365-2a23-111a-e063-dadaa90a10e2Zen Hand Sanitizer
73048-002-032024-01-30C16284748780-11030e365-2a23-111a-e063-dadaa90a10e2Zen Hand Sanitizer
73048-002-042024-01-30C16284748780-11030e365-2a23-111a-e063-dadaa90a10e2Zen Hand Sanitizer
73048-002-052024-01-30C16284748780-11030e365-2a23-111a-e063-dadaa90a10e2Zen Hand Sanitizer

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73048-00273048-002-01, 73048-002-02, 73048-002-03, 73048-002-04, 73048-002-05

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
GLYCERINPDC6A3C0OXIACT
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MACTIB
ALPHA-TOCOPHEROLH4N855PNZ1IACT

Source Document#

Source XML · Source PDF

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
1d937f9a-0848-76dd-e063-6394a90aba3ea5017e93-715e-d1ab-e053-2995a90a0dfe2024-07-19WarningsExact identifier
spl set id: a5017e93-715e-d1ab-e053-2995a90a0dfe

Reported adverse events (FAERS/openFDA)#

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