Dosage and administration
Apply to hands thoroughly and rub vigorously until dry. For children under 6 years, use only with adult supervision. Not recommended for infants.
SUPPRESS Hand Sanitizer
- Manufacturer
- HD Group LLC
- Effective date
- 2022-01-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:46:59
Label at a glance#
ProductSUPPRESS Hand Sanitizer
Active ingredientALCOHOL
Label structure13 sections
Storage and handling
Do not store above 104F (40C) May discolor some fabrics harmful to some wood finishes
Label contents#
Full prescribing information#
Active Ingredient(s)
Alcohol 75% v/v. Purpose: Antiseptic
Purpose
Antiseptic, Hand Sanitizer
Use
to decrease bacteria on the skin.
Warnings
For external use only. Do not inhale or ingest. Flammable. Keep away from heat or flame when using this product.
Do not use
- in children less than 2 months of age
- on open skin wounds
OTC - WHEN USING SECTION
When using this product keep away from eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin.
OTC - STOP USE SECTION
Stop use and ask a physician if skin irritation occurs.
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 immediately.
Directions
- Apply to hands thoroughly and rub vigorously until dry.
- For children under 6 years, use only with adult supervision.
- Not recommended for infants.
Other information
- Do not store above 104F (40C)
- May discolor some fabrics
- harmful to some wood finishes
Inactive ingredients
purified water USP
PEG-40 hydrogenated castor oil
carbomer
sodium hydroxide
aloe vera extract
Package Label - Principal Display Panel
500 mL NDC: 77343-111-01
Distributed By:
Distributed by: HD Group LLC 335 N Edgewood Ln, Suite 130 Eagle, ID 83616
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 77343-111-01 | 2024-01-30 | C162847 | 48780-1 | 1030e365-3c93-111a-e063-dadaa90a10e2 | SUPPRESS Hand Sanitizer |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 77343-111-01 | SUPPRESS Hand Sanitizer | 500 mL in 1 BOTTLE | GEL | 500 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- SUPPRESS Hand Sanitizer
- ALCOHOL
- SODIUM HYDROXIDE
- ALOE VERA LEAF
- PEG-40 CASTOR OIL
- CARBOMER 940
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 77343-111 | 77343-111-01 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SODIUM HYDROXIDE | 55X04QC32I | IACT |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| PEG-40 CASTOR OIL | 4ERD2076EF | IACT |
| CARBOMER 940 | 4Q93RCW27E | 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 |
|---|---|---|---|---|---|---|
| d590c24a-b555-4fc5-e053-2995a90a7c9d | abb0a9ae-24bb-edbd-e053-2995a90a1265 | 2022-01-14 | Warnings | d590c24a-b555-4fc5-e053-2995a90a7c9d abb0a9ae-24bb-edbd-e053-2995a90a1265 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.