Dosage and administration
Wet hands thoroughly with product and allow to dry without wiping. Supervise children under 6 years of age when using this product to avoid swallowing.
Hand Sanitizer
- Manufacturer
- GreenSupply.com LLC
- Effective date
- 2020-10-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:31:34
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
Label contents#
Full prescribing information#
Active Ingredient(s)
Ethyl Alcohol 75% v/v. Purpose: Antimicrobial
Purpose
Antimicrobial, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
- in children less than 2 months of age
- on open skin wounds
OTC - WHEN USING SECTION
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation occurs. These may be signs of a serious condition.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
OTC - STOP USE SECTION
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
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 right away.
Directions
- Wet hands thoroughly with product and allow to dry without wiping.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Inactive ingredients
water (aqua), glycerin, propylene glycol, carbomer, aminomethylpropanol, aloe vera leaf, alpha-tocopheryl acetate (vitamin e)
Package Label - Principal Display Panel
100 mL NDC: 74796-002-01
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 74796-002-01 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-b23d-a426-e053-dadaa90af4c2 | Green Supply Updated Formula |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74796-002-01 | Hand Sanitizer | 100 mL in 1 BOTTLE | SPRAY | 100 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ALCOHOL
- ALPHA-TOCOPHEROL ACETATE
- PROPYLENE GLYCOL
- GLYCERIN
- AMINOMETHYLPROPANOL
- WATER
- ALOE VERA LEAF
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 74796-002 | 74796-002-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALPHA-TOCOPHEROL ACETATE | 9E8X80D2L0 | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE | 0A5MM307FC | 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 |
|---|---|---|---|---|---|---|
| b18f0297-b0eb-610a-e053-2995a90afdce | b18f04d4-725f-5cdc-e053-2995a90ad427 | 2020-10-12 | Warnings | b18f0297-b0eb-610a-e053-2995a90afdce b18f04d4-725f-5cdc-e053-2995a90ad427 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.