Dosage and administration
Put enought product in your palm to cover all surfaces of both hands and rub hands together briskly until dry. children under 6 years of age should be supervised when using this product.
Aloe Vera Hand Sanitizer w/Fragrance
- Manufacturer
- L.O.D.C. Group, Ltd. | Lily of the Desert
- Effective date
- 2021-07-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:41:27
Label at a glance#
ProductAloe Vera Hand Sanitizer w/Fragrance
Active ingredientALCOHOL
Label structure12 sections
Storage and handling
Store below 110F
Label contents#
Full prescribing information#
Purpose
Hand sanitizer to help reduce bacteria on the skin
Use
hand sanitizer to help reduce bacteria on the skin
Warnings
Flammable. Keep away from heat or flame.
For external use only.
OTC - WHEN USING SECTION
When using this product do not use in or near the eyes. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash appears and lasts..
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 appears and lasts.
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
- Put enought product in your palm to cover all surfaces of both hands and rub hands together briskly until dry.
- children under 6 years of age should be supervised when using this product.
Other information
- Store below 110F
Inactive ingredients
Aloe Vera Leaf Juice (Organic), Ammonium Polyacryloyl Dimethyl Taurate, Caprylyl Glycol, Fragrance, Glycerin, Isopropyl Myristate, Tocopheryl Acetate (Vitamin E), Water (Aqua)
Active Ingredient(s)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
RECENT MAJOR CHANGES SECTION
Initial issue
Package Label - Principal Display Panel
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 79949-001-01 | 2023-01-30 | C162847 | 48780-1 | f386c64a-457f-0266-e053-dadaa90a7c1a | a4730626-3124-662d-e053-2a95a90a0c1f |
| 79949-001-02 | 2023-01-30 | C162847 | 48780-1 | f386c64a-457f-0266-e053-dadaa90a7c1a | a4730626-3124-662d-e053-2a95a90a0c1f |
| 79949-001-03 | 2023-01-30 | C162847 | 48780-1 | f386c64a-457f-0266-e053-dadaa90a7c1a | a4730626-3124-662d-e053-2a95a90a0c1f |
| 79949-001-04 | 2023-01-30 | C162847 | 48780-1 | f386c64a-457f-0266-e053-dadaa90a7c1a | a4730626-3124-662d-e053-2a95a90a0c1f |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79949-001-01 | Aloe Vera Hand Sanitizer w/Fragrance | 51.3338 g in 1 BOTTLE | GEL | 51.3338 | 2 | |
| 79949-001-02 | Aloe Vera Hand Sanitizer w/Fragrance | 205.3352 g in 1 BOTTLE | GEL | 205.3352 | 2 | |
| 79949-001-03 | Aloe Vera Hand Sanitizer w/Fragrance | 3285.363 g in 1 BOTTLE, DISPENSING | GEL | 3285.363 | 2 | |
| 79949-001-04 | Aloe Vera Hand Sanitizer w/Fragrance | 410.6704 g in 1 BOTTLE | GEL | 410.6704 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Aloe Vera Hand Sanitizer w/Fragrance
- ALCOHOL
- GLYCERIN
- ALOE VERA LEAF
- WATER
- CAPRYLYL GLYCOL
- AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S)
- ISOPROPYL MYRISTATE
- .ALPHA.-TOCOPHEROL ACETATE, DL-
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 79949-001 | 79949-001-01, 79949-001-03, 79949-001-02, 79949-001-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| CAPRYLYL GLYCOL | 00YIU5438U | IACT |
| AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) | F01RIY4371 | IACT |
| ISOPROPYL MYRISTATE | 0RE8K4LNJS | IACT |
| .ALPHA.-TOCOPHEROL ACETATE, DL- | WR1WPI7EW8 | 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 |
|---|---|---|---|---|---|---|
| c70404af-23af-8c33-e053-2995a90a1377 | a4730626-3124-662d-e053-2a95a90a0c1f | 2021-07-13 | Warnings | c70404af-23af-8c33-e053-2995a90a1377 a4730626-3124-662d-e053-2a95a90a0c1f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.