Aloesept HS
- Manufacturer
- Walter G. Legge Company, Inc.
- Effective date
- 2022-09-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:53:03
Label at a glance#
ProductAloesept HS
Active ingredientALCOHOL
Label structure9 sections
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient
Ethyl Alcohol 70% v/v
OTC - PURPOSE SECTION
Purpose
Antiseptic
INDICATIONS & USAGE SECTION
Uses
- For handwashing to decrease bacteria on the skin after changing diapers, assisting ill persons, or before contact with a person under medical care or treatment.
- Recommended for repeated use.
WARNINGS SECTION
Warnings
- For external use only.
OTC - WHEN USING SECTION
Keep out of eyes, ears, or mouth.
OTC - STOP USE SECTION
- Discontinue use if irritation occurs.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
- Keep out of reach of children.
OTHER SAFETY INFORMATION
FLAMMABLE, KEEP AWAY FROM FIRE OR FLAME.
DOSAGE & ADMINISTRATION SECTION
Directions
- If hands are visibly soiled, wash with soap and water and dry hands.
- Wet hands thoroughly with product, especially the area under the fingernails and allow to dry without rinsing.
INACTIVE INGREDIENT SECTION
Inactive ingredients benzalkonium chloride, chlorhexidine gluconate, isopropyl alcohol, PEG 10 dimethicone, PEG-14M, phenoxyethanol, polyquaternium 10, water.
SPL UNCLASSIFIED SECTION
Sold By: Walter G. Legge Company Inc.
444 Central Avenue, Peekskill, N.Y. 10566
1-800-345-3443
MADE IN THE USA
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ALOESEPT HS
WATERLESS HAND SANITIZER
Compliant with CDC Hand Hygiene Guidelines.
Kills more than 99.99% of germs in 15 seconds.
Does not contain DEA/MEA, triclosan, parabens, formaldehyde, dyes or fragrances.
CONTAINS MOISTURIZING AGENTS
1000 ml
Products#
Every source-derived product name is available through these pages.
- Aloesept HS
- Ethanol
- BENZALKONIUM CHLORIDE
- CHLORHEXIDINE GLUCONATE
- ISOPROPYL ALCOHOL
- PEG-10 DIMETHICONE (600 CST)
- POLYETHYLENE OXIDE 600000
- PHENOXYETHANOL
- POLYQUATERNIUM-10 (1000 MPA.S AT 2%)
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 63647-001 | 63647-001-18, 63647-001-34 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BENZALKONIUM CHLORIDE | F5UM2KM3W7 | IACT |
| CHLORHEXIDINE GLUCONATE | MOR84MUD8E | IACT |
| ISOPROPYL ALCOHOL | ND2M416302 | IACT |
| PEG-10 DIMETHICONE (600 CST) | 8PR7V1SVM0 | IACT |
| POLYETHYLENE OXIDE 600000 | 2126FD486L | IACT |
| PHENOXYETHANOL | HIE492ZZ3T | IACT |
| POLYQUATERNIUM-10 (1000 MPA.S AT 2%) | GMR4PEN8PK | IACT |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
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 |
|---|---|---|---|---|---|---|
| e99b4b38-5abf-3ccd-e053-2a95a90a1bc0 | bfa4bb42-ba15-202d-e053-2995a90a105a | 2022-09-26 | Warnings | e99b4b38-5abf-3ccd-e053-2a95a90a1bc0 bfa4bb42-ba15-202d-e053-2995a90a105a |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.