Hand Sanitizer

Manufacturer
Zhejiang Ayan Biotech Co.,Ltd.
Effective date
2024-11-06
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:35:01

Label at a glance#

ProductHand Sanitizer
Active ingredientALCOHOL
Label structure10 sections

Indications and uses

For Hand Sanitizing

Dosage and administration

Wet hands thoroughly with product and allow to dry without wiping. For children under 6 use only under adult Supervision Not recommender for infants

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ethyl alcohol 70%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For Hand Sanitizing

Warnings

WARNINGS SECTION

For external use only-hands.

Flammable.Keep away from heat and flame.

When using this product

OTC - WHEN USING SECTION

  • Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
  • Avoid contact with broken skin.
  • Do not inhale or ingest.

Stop use and ask a doctor 

OTC - STOP USE SECTION

  • if skin irritation or develops.

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.
  • For children under 6 use only under adult Supervision
  • Not recommender for infants

Other information

SPL UNCLASSIFIED SECTION

  • Do not store above 105°F.
  • May discolor some fabrics.
  • Harmful to wood finishes and plastics.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label3Label3

Package Labeling: 15ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label4Label4

Package Labeling: 53ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label5Label5

Package Labeling: 60ml

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN5
581662ethanol 0.7 ML/ML Topical GelSCD5
581662ethanol 70 % Topical GelSY5
581662ethyl alcohol 70 % Topical GelSY5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70412-194-15Hand Sanitizer15 mL in 1 BOTTLEGEL155
70412-194-53Hand Sanitizer53 mL in 1 BOTTLEGEL535
70412-194-60Hand Sanitizer60 mL in 1 BOTTLEGEL605
70412-194-73Hand Sanitizer473 mL in 1 BOTTLEGEL4735

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70412-194HAND SANITIZER (ALCOHOL) GEL [ZHEJIANG AYAN BIOTECH CO.,LTD.]5Current NDC, Legacy NDC, 4 package rows20241108_aec30cdb-6e95-4790-9c47-93202cc17dab.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
70412-19470412-194-73, 70412-194-15, 70412-194-53, 70412-194-60

Ingredients#

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

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

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
Hand SanitizerALCOHOLZhejiang Ayan Biotech Co.,Ltd.aec30cdb-6e95-4790-9c47-93202cc17dab2024-11-06WarningsExact identifier
ndc (package): 70412-194-15
ndc (package): 70412-194-73
ndc (package): 70412-194-60
ndc (package): 70412-194-53
ndc (product): 70412-194
ndc11 (package): 70412019460
ndc11 (package): 70412019453
ndc11 (package): 70412019473
ndc11 (package): 70412019415
spl id: 2641ed70-dbdf-8e5f-e063-6294a90a34d6
spl set id: aec30cdb-6e95-4790-9c47-93202cc17dab

Reported adverse events (FAERS/openFDA)#

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