Dosage and administration
Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.
Aloe Gel
- Manufacturer
- Commercial Beverage Concepts, LLC
- Effective date
- 2020-10-06
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:31:10
Label at a glance#
ProductAloe Gel
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)
Alcohol 70% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame. Do not ingest or inhale.
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.
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
- Place enough product on hands to cover all surfaces. Rub hands together until dry.
- 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
Fragrance (Parfum), Glycerin, Isopropyl Myristate, Polyethylene Glycol/Acrylates Copolymer, Tocopheryl Acetate, Water
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
945.35mL NDC: 75594-071-09
1.89L NDC: 75594-071-10
3.78L NDC: 75594-071-11
237mL NDC: 75594-071-01
354mL NDC:75594-071-03
946mL NDC: 75594-071-04
1.89L NDC: 75594-071-05
3.78L NDC: 75594-071-06
208.198L NDC: 75594-071-07
354mL NDC: 75594-071-16
237mL NDC: 75594-071-17
59ml NDC: 75594-071-18
118ml NDC: 75594-071-19
237ml NDC: 75594-071-20
355ml NDC: 75594-071-21
473ml NDC: 75594-071-22
946ml NDC: 75594-071-23
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75594-071-01 | Aloe Gel | 0.237 L in 1 BOTTLE, PUMP | GEL | 0.237 | 2 | |
| 75594-071-03 | Aloe Gel | 0.473 L in 1 BOTTLE, PUMP | GEL | 0.473 | 2 | |
| 75594-071-04 | Aloe Gel | 0.946 L in 1 BOTTLE, PUMP | GEL | 0.946 | 2 | |
| 75594-071-05 | Aloe Gel | 1.89 L in 1 BOTTLE, PUMP | GEL | 1.89 | 2 | |
| 75594-071-06 | Aloe Gel | 3.78 L in 1 BOTTLE, PUMP | GEL | 3.78 | 2 | |
| 75594-071-07 | Aloe Gel | 208.198 L in 1 DRUM | GEL | 208.198 | 2 | |
| 75594-071-09 | Aloe Gel | 0.94635 L in 1 BOTTLE, PUMP | GEL | 0.94635 | 2 | |
| 75594-071-10 | Aloe Gel | 1.89 L in 1 BOTTLE, PUMP | GEL | 1.89 | 2 | |
| 75594-071-11 | Aloe Gel | 3.78 L in 1 BOTTLE, PUMP | GEL | 3.78 | 2 | |
| 75594-071-16 | Aloe Gel | 0.354 L in 1 BOTTLE, PUMP | GEL | 0.354 | 2 | |
| 75594-071-17 | Aloe Gel | 0.237 L in 1 BOTTLE, DISPENSING | GEL | 0.237 | 2 | |
| 75594-071-18 | Aloe Gel | 0.59 L in 1 BOTTLE, DISPENSING | GEL | 0.59 | 2 | |
| 75594-071-19 | Aloe Gel | 0.118 L in 1 BOTTLE, DISPENSING | GEL | 0.118 | 2 | |
| 75594-071-20 | Aloe Gel | 0.237 L in 1 BOTTLE, PUMP | GEL | 0.237 | 2 | |
| 75594-071-21 | Aloe Gel | 0.355 L in 1 BOTTLE, PUMP | GEL | 0.355 | 2 | |
| 75594-071-22 | Aloe Gel | 0.473 L in 1 BOTTLE, PUMP | GEL | 0.473 | 2 | |
| 75594-071-23 | Aloe Gel | 0.946 L in 1 BOTTLE, PUMP | GEL | 0.946 | 2 | |
| 75594-071-24 | Aloe Gel | 1.89 L in 1 BOTTLE, PUMP | GEL | 1.89 | 2 | |
| 75594-071-25 | Aloe Gel | 3.78 L in 1 BOTTLE, PUMP | GEL | 3.78 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Aloe Gel
- ALCOHOL
- ISOPROPYL MYRISTATE
- GLYCERIN
- .ALPHA.-TOCOPHEROL ACETATE, DL-
- RAPIDGEL EZ1
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75594-071 | 75594-071-09, 75594-071-10, 75594-071-11, 75594-071-01, 75594-071-03, 75594-071-04, 75594-071-05, 75594-071-06, 75594-071-07, 75594-071-16, 75594-071-17, 75594-071-18, 75594-071-19, 75594-071-20, 75594-071-21, 75594-071-22, 75594-071-23, 75594-071-24, 75594-071-25 |
| 74221-004 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, DL- | WR1WPI7EW8 | IACT |
| RAPIDGEL EZ1 | 33JH4A7R2K | IACT |
| 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 |
|---|---|---|---|---|---|---|
| b1084862-e1ff-5bec-e053-2a95a90a1721 | ab25012a-8469-31bf-e053-2a95a90a9fee | 2020-10-06 | Warnings | b1084862-e1ff-5bec-e053-2a95a90a1721 ab25012a-8469-31bf-e053-2a95a90a9fee |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.