Storage and handling
Store between 59-86°f. DO NOT store in heat above 105°f. May discolor some fabrics
LiquidProof Hand Sanitizer GEL
- Manufacturer
- Four Fathers Distillery LLC
- Effective date
- 2020-10-02
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:31:09
Label at a glance#
ProductLiquidProof Gel Hand Sanitizer
Active ingredientALCOHOL
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient(s): Alcohol (ethanol) 70%.
OTC - PURPOSE SECTION
Purpose Antiseptic
INDICATIONS & USAGE SECTION
Use(s): Helps reduce bacteria that can potentially become disease.
WARNING
For external use only. FLAMMABLE: Keep away from heat and flame. DO NOT USE: On children less than 2 months of age. DO NOT USE: On open skin wounds. Keep out of eyes, ears, and mouth. Stop use if rash or irritation occurs. This could be a sign of a serious condition.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children. If swallowed contact doctor or poison control right away.
DOSAGE & ADMINISTRATION SECTION
Directions: Place enough product on hands to cover all surfaces, rub together until dry. Supervise children under 6 years of age to prevent swallowing.
Other Information:
Store between 59-86°f. DO NOT store in heat above 105°f. May discolor some fabrics
INACTIVE INGREDIENT SECTION
Inactive ingredient(s): Glycerin, Aloe Barbadensis Leaf Juice, Hydroxyethylcellulose, Purified Water, Essential Oils
SPL UNCLASSIFIED SECTION
Alcohol Antiseptic 70%/Topical Solution
MADE IN USA
Produced & Bottled By Four Fathers Distillery
2917 Borden St., Jacksonville, FL 32209
FOUR FATHERS Distillery, Jacksonville, Florida
For questions, concerns or help please call the distillery at 904-710-6150
Packaging
DailyMed RxNorm Mappings#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 7792dadb-52b6-46b6-8fdf-80b1171065b5 | Product name | 1 | 20180810 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 78829-500-81 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-b07b-a426-e053-dadaa90af4c2 | LiquidProof Hand Sanitizer GEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 78829-500-81 | LiquidProofGel Hand Sanitizer | 3785 mL in 1 JUG | GEL | 3785 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- LiquidProof Gel Hand Sanitizer
- Alcohol
- GLYCERIN
- ALOE VERA LEAF
- HYDROXYETHYL CELLULOSE, UNSPECIFIED
- WATER
- PEPPERMINT OIL
- EUCALYPTUS OIL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 78829-500 | 78829-500-81 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| GLYCERIN | PDC6A3C0OX | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| HYDROXYETHYL CELLULOSE, UNSPECIFIED | T4V6TWG28D | IACT |
| WATER | 059QF0KO0R | IACT |
| PEPPERMINT OIL | AV092KU4JH | IACT |
| EUCALYPTUS OIL | 2R04ONI662 | 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 |
|---|---|---|---|---|---|---|
| 08305e8b-a279-4689-8b2a-79130efeff5f | 0d486223-8f86-4126-b70f-e080de00d2a4 | 2020-10-02 | Warnings | 08305e8b-a279-4689-8b2a-79130efeff5f 0d486223-8f86-4126-b70f-e080de00d2a4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.