HAND SANITIZER

Manufacturer
Pacific Bridge Products, Inc | Yuyao Huanyan Daily Chemical Products Co., Ltd
Effective date
2020-04-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:10:30

Label at a glance#

ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections

Indications and uses

helps reduce bacteria that potentially can cause disease helps prevent cross contamination by hand contact recommended for repeated use

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.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

  • helps reduce bacteria that potentially can cause disease
  • helps prevent cross contamination by hand contact
  • recommended for repeated use

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

When using this product

OTC - WHEN USING SECTION

keep out of eyes, and mouth. 

In case of contact with eyes,rinse eyes thoroughly with water.

Stop use and ask a doctor 

OTC - STOP USE SECTION

if irritation or redness 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

  • 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

SPL UNCLASSIFIED SECTION

  • avoid freezing and excessive heat above 40°C(104°F)
  • may discolor certain fabrics

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, Aloe Barbadensis Extract, Triethanolamine, Propylene Glycol, Carbomer, Fragrance, Tocopherol.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
581662ethanol 70 % Topical GelPSN1
581662ethanol 0.7 ML/ML Topical GelSCD1
581662ethanol 70 % Topical GelSY1
581662ethyl alcohol 70 % Topical GelSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74730-002-082023-01-30C16284748780-1f386c649-a7de-0266-e053-dadaa90a7c1aHAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
74730-002-08HAND SANITIZER236 mL in 1 BOTTLEGEL2361

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
74730-002HAND SANITIZER (ALCOHOL) GEL [PACIFIC BRIDGE PRODUCTS, INC]1Legacy NDC, 1 package rows20200510_7c52102d-8b11-45f1-9e8a-9712412eeb0b.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
74730-00274730-002-08

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

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
a445094f-5887-7c70-e053-2a95a90a31837c52102d-8b11-45f1-9e8a-9712412eeb0b2020-04-27WarningsExact identifier
spl id: a445094f-5887-7c70-e053-2a95a90a3183
spl set id: 7c52102d-8b11-45f1-9e8a-9712412eeb0b

Reported adverse events (FAERS/openFDA)#

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