Dosage and administration
-place enough product on hands to cover all surfaces. Rub hands together until dry. -Supervise children under 6 years of agen when using this product to avoid swallowing.
RCD Hand Sanitizer
- Manufacturer
- Rush Creek Distilling, LLC
- Effective date
- 2020-03-27
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:38:29
Label at a glance#
ProductRCD Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections
Label contents#
Full prescribing information#
Drug Facts - Active Ingredients
Drug Facts - Purpose
Antiseptic
Drug Facts - Warning
For external use only. Flammable. Keep away from heat or flame.
Drug Facts - Do not Use
- in children less than 2 months of age
- on open skin wounds
Drug Facts - When Using ths Product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Drug Facts - Stop Use and ask a doctor
if irritation or rash occurs. These may be signs of a serious condition.
Drug Facts - Keep out of reach of children
if swallowed, get medical help or contact a Poison Control Center right away.
Drug Facts - Directions
-place enough product on hands to cover all surfaces. Rub hands together until dry.
-Supervise children under 6 years of agen when using this product to avoid swallowing.
Drug Facts - Other Information
- Store between 15-30C (59-86F)
- Avoid freezing and excessive heat above 40C (104F)
Drug Facts - Inactive Ingredients
glycerin, hydrogen peroxide, purified water USP
DOSAGE & ADMINISTRATION SECTION
Front/Main Label
Product Description - Hand Sanitizer
Active Ingredent - Denatured Ethanol 80%
Size in mL - this will vary depending on the package size per packagin NDC
Manufacturing location and contact information
FDA-Initiated Inactive NDC Indexing#
Products#
Every source-derived product name is available through these pages.
- RCD Hand Sanitizer
- Hand Sanitizer
- HYDROGEN PEROXIDE
- GLYCERIN
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 73977-001 | 73977-001-01, 73977-001-02, 73977-001-03, 73977-001-05, 73977-001-10, 73977-001-19, 73977-001-38 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| HYDROGEN PEROXIDE | BBX060AN9V | IACT |
| GLYCERIN | PDC6A3C0OX | 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 |
|---|---|---|---|---|---|---|
| 2902733f-774a-8cc5-e063-6394a90a2739 | a1b0eebf-9f89-2c2b-e053-2995a90a22e0 | 2024-12-11 | Warnings | a1b0eebf-9f89-2c2b-e053-2995a90a22e0 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.