Storage and handling
Do not store about 110°F. Harmful to wood finishes and plastics.
Koi Hand Sanitizer
- Manufacturer
- Koi CBD LLC | Brad Ridenour
- Effective date
- 2020-04-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:06:13
Label at a glance#
ProductKoi Hand Sanitizer
Active ingredientALCOHOL
Label structure10 sections
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Ethyl Alcohol 62%...... Antimicrobial
OTC - PURPOSE SECTION
Antimicrobial
INDICATIONS & USAGE SECTION
Hand sanitizer to help decrease bacteria on the skin. Recommended for repeat use.
WARNINGS SECTION
For external use only. Flammable, keep away from fire or flames.
OTC - DO NOT USE SECTION
Do not use in eyes. In case of contact, rinse thoroughly with water.
OTC - STOP USE SECTION
Stop use and consult a doctor if irritation and redness develop and persist for more than 72 hours.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.
DOSAGE & ADMINISTRATION SECTION
Wet hands thoroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision. Not recommended for infants.
STORAGE AND HANDLING SECTION
Do not store about 110°F. Harmful to wood finishes and plastics.
INACTIVE INGREDIENT SECTION
Deionized Water, Glycerin, Propylene Glycol, Organic Aloe Barbadensis (Aloe Vera) Leaf Extract, Panthenol (Pro-Vitamin B5), Tocopheryl Acetate (Vitamin E Acetate), Carbomer, Aminomethyl Propanol, Fragrance.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
59 mL NDC: 73842-002-01
DailyMed RxNorm Mappings#
Product Linked Resources#
| Resource | Code type | Value | Equivalent identifiers | Source image |
|---|---|---|---|---|
| Barcode | EAN-13 | 0857321007207 | GTIN-13: 0857321007207 EAN-13: 0857321007207 GTIN-12: 857321007207 UPC-A: 857321007207 GTIN storage (14 digits): 00857321007207 | Sanitizer Principal Display.jpg |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 73842-002-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-6ebf-a426-e053-dadaa90af4c2 | Koi Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73842-002-01 | Koi Hand Sanitizer | 59 mL in 1 BOTTLE, PUMP | GEL | 59 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Koi Hand Sanitizer
- Ethyl Alcohol, 62%
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
- PROPYLENE GLYCOL
- ALCOHOL
- ALPHA-TOCOPHEROL ACETATE
- AMINOMETHYLPROPANOL
- WATER
- GLYCERIN
- ALOE VERA LEAF
- PANTHENOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73842-002 | 73842-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PANTHENOL | WV9CM0O67Z | 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 |
|---|---|---|---|---|---|---|
| a33a7691-ceb7-a579-e053-2995a90a64d5 | a33a7691-ceb6-a579-e053-2995a90a64d5 | 2020-04-14 | Warnings | a33a7691-ceb7-a579-e053-2995a90a64d5 a33a7691-ceb6-a579-e053-2995a90a64d5 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.