CA Global Wave Sanitizer Gel 75

Manufacturer
C & A MARKETING, INC.
Effective date
2020-06-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 23:19:12

Label at a glance#

ProductWave Hand Sanitizer
Active ingredientALCOHOL
Label structure12 sections

Indications and uses

■ Hand Sanitizer to help reduce bacteria on the skin. For use when soap and water are not available

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 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Alcohol 75%v/v

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

■ Hand Sanitizer 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

Do not use

OTC - DO NOT USE SECTION

■ on children less than 2 months of age ■ on open skin wounds

When using this product

OTC - WHEN USING SECTION

keep out of eyes, ears, ears and mouth. In case of eye contact immediately flush eyes thoroughly with water

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash occurs. These may be the signs of a serious condition.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidentail ingestion, contact a doctor or Poison Control Center immediately.

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 15º-30ºC (59º-89ºF) ■ Avoid freezing and excessive heat above 40ºC (104ºF) ■ May discolor fabrics or surfaces.

Inactive ingredients

INACTIVE INGREDIENT SECTION

■ Glycerin, hydroxypropyl cellulose, water

Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package labelpackage label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1305100ethanol 75 % Topical GelPSN2
1305100ethanol 0.75 ML/ML Topical GelSCD2
1305100ethanol 75 % Topical GelSY2

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78754-001-08Wave Hand Sanitizer237 mL in 1 BOTTLE, PLASTICGEL2372
78754-001-16Wave Hand Sanitizer500 mL in 1 BOTTLE, PLASTICGEL5002
78754-001-28Wave Hand Sanitizer3790 mL in 1 BOTTLE, PLASTICGEL37902

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78754-001WAVE HAND SANITIZER (ALCOHOL) GEL [C & A MARKETING, INC.]2Legacy NDC, 3 package rows20200627_a84dfb7f-c453-4d01-e053-2995a90af0e6.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78754-00178754-001-08, 78754-001-16, 78754-001-28

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
a8fe89e5-023f-7b99-e053-2a95a90a2dc4a84dfb7f-c453-4d01-e053-2995a90af0e62020-06-26WarningsExact identifier
spl id: a8fe89e5-023f-7b99-e053-2a95a90a2dc4
spl set id: a84dfb7f-c453-4d01-e053-2995a90af0e6

Reported adverse events (FAERS/openFDA)#

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