Indications and uses
To decrease bacteria on the skin that could cause disease. recommended for repeat use
not have
- Manufacturer
- Shandong Aoyou Biotechnology Co.,Ltd
- Effective date
- 2020-05-04
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:10:33
Label at a glance#
Productnot have
Active ingredientALCOHOL
Label structure11 sections
Dosage and administration
wet hands to thoroughly with product and allow to dry without wiping. for children under 6,use only under adult supervision. not recommend for infants.
Storage and handling
do not store above 105F. may discolor some fabric. harmful to wood finishes and plastic.
Label contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 70%vv
Purpose
Antimicrobial
Uses
To decrease bacteria on the skin that could cause disease.
recommended for repeat use
Warnings
For external use only:hands.
Flammable, Keep away from fire or flame.
When using this product
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
Stop using and ask a doctor If irritation or redness develops
condition persists for more than 72 hours
Keep out of reach of children
if swallowed,get medical help or contact a Poison Control Center right away.
Directions
wet hands to thoroughly with product and allow to dry without wiping.
for children under 6,use only under adult supervision.
not recommend for infants.
Other Information
do not store above 105F.
may discolor some fabric.
harmful to wood finishes and plastic.
Inactive Ingredients
purified water
Package Label - Principal Display Panel
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75118-001-01 | 2021-07-23 | C162847 | 48780-1 | c7ccaba7-144c-fd44-e053-dadaa90aa01b | Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75118-001-01 | not have | 425 mL in 1 BOTTLE | GEL | 425 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- not have
- Hand Sanitizer
- ALCOHOL
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75118-001 | 75118-001-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| WATER | 059QF0KO0R | IACT |
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 |
|---|---|---|---|---|---|---|
| a4cfa152-62b9-693e-e053-2995a90aff75 | a5356ee0-a696-5226-e053-2a95a90af960 | 2020-05-04 | Warnings | a4cfa152-62b9-693e-e053-2995a90aff75 a5356ee0-a696-5226-e053-2a95a90af960 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.