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.
Hand Sanitizer
- Manufacturer
- ZHEJIANG JINGHUI COSMETICS SHARE CO.,LTD
- Effective date
- 2024-04-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 6
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:05:03
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections
Storage and handling
Do not store above 105°F May discolor some fabrics Harmful to wood finishes and plastics
Label contents#
Full prescribing information#
Purpose
Alcohol 70% v/v. Purpose: Antiseptic
Use
to decrease bacteria on the skin that could cause disease
recommended for repeated use
Warnings
For external use only
Flammable
Keep away from fire or flame
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
OTC - STOP USE SECTION
irritation or redness develops
condition persists for more than 72 hours
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
If swallowed,get medical help or contact a Poison Control Center right away.
Directions
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
Do not store above 105°F
May discolor some fabrics
Harmful to wood finishes and plastics
Inactive ingredients
water, Acrylates Copolymer,Propylene Glycol,Butylene Glycol,Aminomethyl Propanol,Fragrance.
Active ingredient
Alcohol 70% v/v. Purpose: Antiseptic
Package label, principal Display Panel
75mL NDC: 73905-019-01
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- Ethyl Alcohol
- BUTYL ACRYLATE
- DENATONIUM
- WATER
- BUTYLENE GLYCOL
- AMINOMETHYLPROPANOL
- PROPYLENE GLYCOL
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73905-019 | 73905-019-01, 73905-019-02, 73905-019-03 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BUTYL ACRYLATE | 705NM8U35V | IACT |
| DENATONIUM | 4IK22DF4OU | IACT |
| WATER | 059QF0KO0R | IACT |
| BUTYLENE GLYCOL | 3XUS85K0RA | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
Source Document#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 165f851c-5c95-d9af-e063-6394a90aedb1 | a6250431-e7ed-3df1-e053-2a95a90a1659 | 2024-04-18 | Warnings | 165f851c-5c95-d9af-e063-6394a90aedb1 a6250431-e7ed-3df1-e053-2a95a90a1659 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.