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
- SUN WAVE WELLNESS, LLC
- Effective date
- 2020-07-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-05-31 23:25:53
Label at a glance#
ProductHAND SANITIZER
Active ingredientALCOHOL
Label structure7 sections
Label contents#
Full prescribing information#
Use(s)
To help reduce bacteria on the skin. For use when soap and water are not available.
Warnings
For external use only.
Flammable. Keep away from heat or flame.
Do not use
- on children less than 2 months of age
- on open skin wounds
- around eyes
- in ears and mouth
When using this product
keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
- avoid contact with broken skin
- do not inhale or ingest
Stop use and ask a doctor if
irritation or rash occurs.
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 or excessive heat above 40C (104F).
Inactive ingredients
Aloe Barbadensis (leaf) Extract, Fragrance, Glycerin, Purified Water
Manufactured by:
Sun Wave Wellness, LLC
1419 Chaffee Drive #101
Titusville, FL 32780-7933
Drug Facts
Active Ingredient(s)
Alcohol 70% v/v
Purpose
Antiseptic
DailyMed RxNorm Mappings#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 75023-005-04 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-6085-a426-e053-dadaa90af4c2 | VERSION2: THIS IS INTENDED TO CORRECT AND REPLACE VERSION 1 OF SETID ITEM ENDING "...ADEE2" 2 CORRECTIONS: (1) TITLE (IE, THIS FIELD); (2) BACK LABEL: CONSUMER HAND SANITIZER; NON-EMERGENCY; SPECIALLY DENATURED ETHYL ALCOHOL = DEFERRED GRASE ACTIVE INGREDIENT DETERMINATION EFFECTIVE APRIL 13, 2020; PART333E FOR OTC HAND RUB SANITIZERS (CONSUMER) |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 75023-005-04 | HAND SANITIZER | 1.893 L in 1 BOTTLE | LIQUID | 1.893 | 2 |
DailyMed Dashboard NDC Coverage#
Products#
Every source-derived product name is available through these pages.
- HAND SANITIZER
- DENATURED DT ETHYL ALCOHOL
- WATER
- ALCOHOL
- ALOE VERA LEAF
- LIMONENE, (+)-
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 75023-005 | 75023-005-04 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | ACTIB |
| ALOE VERA LEAF | ZY81Z83H0X | IACT |
| LIMONENE, (+)- | GFD7C86Q1W | IACT |
| GLYCERIN | PDC6A3C0OX | 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 |
|---|---|---|---|---|---|---|
| ad192e16-71c0-7155-e053-2a95a90a57a4 | aa051319-09f1-57d5-e053-2a95a90adee2 | 2020-07-05 | Warnings | ad192e16-71c0-7155-e053-2a95a90a57a4 aa051319-09f1-57d5-e053-2a95a90adee2 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.