Dosage and administration
Place a generous amount of product on hands and rub hands together until dry.
EHS7000-4
- Manufacturer
- Epic Chemistry LLC
- Effective date
- 2020-12-30
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- full-release
- Hydrated at
- 2026-05-31 23:36:19
Label at a glance#
ProductEHS7000-4
Active ingredientALCOHOL
Label structure13 sections
Label contents#
Full prescribing information#
Active Ingredient
Ethyl Alcohol 70.05 v/v% Antimicrobial
Usage
Help reduce bacteria on the skin
Directions
Place a generous amount of product on hands and rub hands together until dry.
Other Information
Do not store above 100° F. May cause fabric discoloration.
Inactive Ingredients
Water (Agua), Sorbitol, Methycellulose, Polyquaternium-10, Fragrance, Glycerin
Dosage
Use a liberal amount in palm of hand.
Notice
Keep out of reach of children.
Indications & Usage
For use when soap and water are not available, or in addition to.
Purpose
To cleanse hands when water and soap are not available.
Warnings
For external use only
Flammable. Keep away from heat or flame.
When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Avoid contact with broken skin. Do not ingest or inhale.
Stop use and ask doctor if skin irritation or redness occurs.
Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.
Warnings
For external use only
Flammable. Keep away from heat or flame.
When using this product avoid contact with eyes. If contact occurs, flush thoroughly with water. Avoid contact with broken skin. Do not ingest or inhale.
Stop use and ask doctor if skin irritation or redness occurs.
Keep out of reach of children. If swallowed, seek medical attention or contact Poison Control Center immediately.
Warnings
Use as directed.
Label
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 77022-1114-4 | 2022-01-28 | C162847 | 48780-1 | d6a99b3a-01de-a426-e053-dadaa90af4c2 | 4 OZ |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 77022-1114-4 | EHS7000-4 | 1 in 1 BOTTLE | GEL | 1 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 77022-1114 | EHS7000-4 GEL [EPIC CHEMISTRY LLC] | 3 | Legacy NDC, 1 package rows | 20210101_af9a64b7-d38f-6822-e053-2995a90aecbd.zip |
Products#
Every source-derived product name is available through these pages.
- EHS7000-4
- ALCOHOL
- METHYLCELLULOSE, UNSPECIFIED
- WATER
- GLYCERIN
- POLYQUATERNIUM-10 (30000 MPA.S AT 2%)
- SORBITOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77022-1114 | 77022-1114-4 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | ACTIB |
| METHYLCELLULOSE, UNSPECIFIED | Z944H5SN0H | IACT |
| WATER | 059QF0KO0R | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
| POLYQUATERNIUM-10 (30000 MPA.S AT 2%) | C7RDC8Y4JS | IACT |
| SORBITOL | 506T60A25R | 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 |
|---|---|---|---|---|---|---|
| b7b0db98-5c72-401a-e053-2a95a90aebee | af9a64b7-d38f-6822-e053-2995a90aecbd | 2020-12-30 | Warnings | b7b0db98-5c72-401a-e053-2a95a90aebee af9a64b7-d38f-6822-e053-2995a90aecbd |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.