Storage and handling
Other information. do not store above 105°F， may discolor some fabics. harmful to wood finished and plastics
Hand Sanitizer
- Manufacturer
- Biolab International Incorporated
- Effective date
- 2020-06-29
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:19:42
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure11 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredients
Ethyl Alcohol 62%
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses hand sanitizer to help reduce bacteria on the skin . For occassional and personal domestic use
WARNINGS SECTION
Warnings
for external use only: hands
Flammable. Keep away from fire or flame
OTC - WHEN USING SECTION
when using this product, avoid contact with eyes, in case of contact, rinse eyes thoroughly with water, avoid contact with broken skin .
OTC - STOP USE SECTION
Stop use and consult a doctor if . irritation or redness develops. condition persists for more than 72 hours
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. children under 6, use only under adult supervision, Not recommended for infants.
For external use only. Do not drink.
If swallowed, seek professional assistance or contact a poison control center.
DOSAGE & ADMINISTRATION SECTION
Directions. Place enough product in your palm to thoroughly spread on both hands and rub into skin until dry.
STORAGE AND HANDLING SECTION
Other information. do not store above 105°F， may discolor some fabics. harmful to wood finished and plastics
INACTIVE INGREDIENT SECTION
Inactive ingredients acrylates/C10-C30 alkyl acrylate crosspolymer,aloe barbadensis leaf juice, glycerin, maltodextrin, propylene glycol, water , triethanolamine,Fragrance. FD&C Blue No.1, FD&C Yellow No.5
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72264-008-01 | 2023-01-30 | C162847 | 48780-1 | f386c64a-0ef8-0266-e053-dadaa90a7c1a | a944e4fa-d519-6f65-e053-2a95a90a98e2 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72264-008-01 | Hand Sanitizer | 236 mL in 1 BOTTLE, PUMP | GEL | 236 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ETHYL ALCOHOL
- TROLAMINE
- MALTODEXTRIN
- PROPYLENE GLYCOL
- WATER
- ALOE VERA LEAF
- GLYCERIN
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- FD&C BLUE NO. 1
- FD&C YELLOW NO. 5
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72264-008 | 72264-008-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| TROLAMINE | 9O3K93S3TK | IACT |
| MALTODEXTRIN | 7CVR7L4A2D | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C YELLOW NO. 5 | I753WB2F1M | 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 |
|---|---|---|---|---|---|---|
| a944e4fa-d51a-6f65-e053-2a95a90a98e2 | a944e4fa-d519-6f65-e053-2a95a90a98e2 | 2020-06-29 | Warnings | a944e4fa-d51a-6f65-e053-2a95a90a98e2 a944e4fa-d519-6f65-e053-2a95a90a98e2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.