Sun Wave Consumer Antiseptic Hand Sanitizer

Manufacturer
SUN WAVE WELLNESS, LLC | SUN WAVE WELLNESS LLC
Effective date
2020-04-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:08:47

Label at a glance#

ProductSun Wave Consumer Antiseptic Hand Sanitizer
Active ingredientISOPROPYL ALCOHOL
Label structure8 sections

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.

Storage and handling

Store between 15-30C (59-86F) Avoid freezing and excessive heat above 40C (104F).

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Isopropyl Alcohol 70% v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Use(s)

INDICATIONS & USAGE SECTION

To help reduce bacteria on the skin. For use when soap and water are not available.

Warnings

WARNINGS SECTION

For external use only.

Flammable. Keep away from heat or flame

OTC - DO NOT USE SECTION

Do not use

  • on children less than 2 months of age
  • on open skin wounds
  • around eyes
  • in ears and mouth

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • 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

STORAGE AND HANDLING SECTION

  • Store between 15-30C (59-86F)
  • Avoid freezing and excessive heat above 40C (104F).

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (leaf) Extract, Fragrance, Glycerin, Purified Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Sanitizer pkg001Sanitizer pkg001ANTISEPTIC

HAND

SANITIZER

SPRAY GEL

ALCOHOL ANTISEPTIC 70%

enriched with aloe

CLEAN SCENT

TOPICAL SOLUTION

KILLS

GERMS &

BACTERIA

3.4OZ 100ML

NO-STERILE SOLUTION

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1014638isopropyl alcohol 70 % Topical SprayPSN1
1014638isopropyl alcohol 0.7 ML/ML Topical SpraySCD1
1014638isopropyl alcohol 70 % Topical SpraySY1

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75023-001-01Sun Wave Consumer Antiseptic Hand Sanitizer100 mL in 1 BOTTLE, SPRAYSPRAY1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75023-001SUN WAVE CONSUMER ANTISEPTIC HAND SANITIZER (ISOPROPYL ALCOHOL) SPRAY [SUN WAVE WELLNESS, LLC]1Legacy NDC, 1 package rows20200430_a2f403a1-6e9b-e2a3-e053-2a95a90ac6f9.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75023-00175023-001-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
a2f324b5-b718-4ec6-e053-2a95a90a77d1a2f403a1-6e9b-e2a3-e053-2a95a90ac6f92020-04-10WarningsExact identifier
spl id: a2f324b5-b718-4ec6-e053-2a95a90a77d1
spl set id: a2f403a1-6e9b-e2a3-e053-2a95a90ac6f9

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.