Clorox Antimicrobial Hand Sanitizer
- Manufacturer
- The Clorox Company | Carroll Company
- Effective date
- 2016-01-25
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 22:44:42
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 62% w/w
OTC - PURPOSE SECTION
Antimicrobial
INDICATIONS & USAGE SECTION
Uses
• To sanitize hands without requiring water or a rinse
WARNINGS SECTION
Warnings
FLAMMABLE
For external use only
OTC - WHEN USING SECTION
When using this product
• do not use near heat or flame
• do not use in or near eyes
• discontinue use if irritation and redness develop, or if condition persists for more than 72 hours
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN. In case of accidental ingestion, seek medical attention or contact a poison control center immediately.
DOSAGE & ADMINISTRATION SECTION
Directions
• Wet hands thoroughly with product and allow to dry without wiping
OTHER SAFETY INFORMATION
Other Information
• Store at room temperature
INACTIVE INGREDIENT SECTION
Inactive ingredients
- Aloe Barbadensis Leaf Juice
- Carbomer
- Diisopropylamine
- FD&C Blue #1
- Fragrance
- Glycerin
- Isopropyl Myristate
- Phenoxyethanol
- Tocopherol Acetate
- Water
OTC - QUESTIONS SECTION
QUESTIONS OR COMMENTS?
Call
1-800-638-2625 or visit
www.hlk.cc
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Clorox Antimicrobial Hand Sanitizer
18 FL OZ (532 mL)
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0044600315188 | GTIN-13: 0044600315188 EAN-13: 0044600315188 GTIN-12: 044600315188 UPC-A: 044600315188 GTIN storage (14 digits): 00044600315188 | 214345.001_PPD_CFB_ProjectSky_HandSanitizer_6_OL_i01.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 26509-0010-8 | 2020-01-31 | C162847 | 48780-1 | 9d75b9d0-268f-f424-e053-dadaa90a57ce | Drug Facts |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 26509-0010-8 | Clorox Antimicrobial Hand Sanitizer | 532 mL in 1 BOTTLE | GEL | 532 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 26509-0010 | CLOROX ANTIMICROBIAL HAND SANITIZER (ETHYL ALCOHOL) GEL [THE CLOROX COMPANY] | 1 | Legacy NDC, 1 package rows | 20160125_2561c0da-3cf8-58b9-e054-00144ff88e88.zip |
Products#
Every source-derived product name is available through these pages.
- Clorox Antimicrobial Hand Sanitizer
- Ethyl Alcohol
- ALCOHOL
- ALOE VERA LEAF
- ISOPROPYL MYRISTATE
- ALPHA-TOCOPHEROL ACETATE
- WATER
- DIISOPROPANOLAMINE
- FD&C BLUE NO. 1
- GLYCERIN
- PHENOXYETHANOL
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 26509-0010 | 26509-0010-8 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| WATER | 059QF0KO0R | IACT |
| DIISOPROPANOLAMINE | 0W44HYL8T5 | IACT |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | 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 |
|---|---|---|---|---|---|---|
| 2561abfd-61dc-562c-e054-00144ff8d46c | 2561c0da-3cf8-58b9-e054-00144ff88e88 | 2016-01-25 | Warnings | 2561abfd-61dc-562c-e054-00144ff8d46c 2561c0da-3cf8-58b9-e054-00144ff88e88 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
