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.
Hand Sanitizer
- Manufacturer
- Fareva Morton Grove, Inc. | Fareva Morton Grove, Inc
- Effective date
- 2020-12-15
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-05-31 23:35:20
Label at a glance#
ProductHand Sanitizer
Active ingredientALCOHOL
Label structure13 sections
Storage and handling
Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F)
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
a. Alcohol (ethanol) (USP or Food Chemical Codex (FCC) grade) (77%, volume/volume (v/v)) in an aqueous solution denatured according to Alcohol and Tobacco Tax and Trade Bureau regulations in 27 CFR part 20.
b. Glycerin
c. FRAGRANCE (PARFUM)
d. ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER
e. ALOE BARBADENSIS LEAF JUICE
f. AMINOMETHYL PROPANOL
g. RED 4 (CI 14700)
h. CITRIC ACID
i. SODIUM BENZOATE
j. POTASSIUM SORBATE
Active Ingredient(s)
Alcohol 78% v/v. Purpose: Antiseptic
Purpose
Antiseptic
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 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 and redness develops and persists.
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
Acrylates/C10-30 Acrylate Crosspolymer, Aloe Barbadensis Leaf Juice, Aminomethyl Propanol, Citric Acid, Fragrance, Glycerin, Potassium Sorbate, Red 4 (CI 14700), Sodium Benzoate, Water
Package Label - Principal Display Panel
50 mL NDC: 72686-188-05
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 72686-188-05 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-4cc0-a426-e053-dadaa90af4c2 | b6872912-265f-3c0b-e053-2995a90aac6c |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 72686-188-05 | Hand Sanitizer | 50 mL in 1 TUBE | GEL | 50 | 1 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- Hand Sanitizer
- ALCOHOL
- AMINOMETHYLPROPANOL
- GLYCERIN
- FRAGRANCE JUNIPERBERRY ORANGE ORC2000843
- WATER
- CARBOMER INTERPOLYMER TYPE A (55000 CPS)
- POTASSIUM SORBATE
- SODIUM BENZOATE
- CITRIC ACID MONOHYDRATE
- ALOE
- FD&C RED NO. 4
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 72686-188 | 72686-188-05 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AMINOMETHYLPROPANOL | LU49E6626Q | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| FRAGRANCE JUNIPERBERRY ORANGE ORC2000843 | 2KS3NF08B2 | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| CARBOMER INTERPOLYMER TYPE A (55000 CPS) | 59TL3WG5CO | IACT |
| POTASSIUM SORBATE | 1VPU26JZZ4 | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| CITRIC ACID MONOHYDRATE | 2968PHW8QP | IACT |
| ALOE | V5VD430YW9 | IACT |
| FD&C RED NO. 4 | X3W0AM1JLX | 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 |
|---|---|---|---|---|---|---|
| b6873468-bbfa-381b-e053-2a95a90a352f | b6872912-265f-3c0b-e053-2995a90aac6c | 2020-12-15 | Warnings | b6873468-bbfa-381b-e053-2a95a90a352f b6872912-265f-3c0b-e053-2995a90aac6c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.