FDA.reportPublic FDA data

WHAT VIRUS

Manufacturer
Champ Products, Ltd
Effective date
2021-02-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:37:57

Label at a glance#

ProductWHAT VIRUS
Active ingredientBENZALKONIUM CHLORIDE
Label structure9 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Rub together until dry without wiping

Dosage and administration

Apply enough product to cover hands. Rub together without wiping.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antiseptic

Uses

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin
Rub together until dry without wiping

Directions

DOSAGE & ADMINISTRATION SECTION

Apply enough product to cover hands.
Rub together without wiping.

Warnings

WARNINGS SECTION

For external use only.

When using this product: avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor: if irritation or redness develops - condition persists for more than 72 hours.

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.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, COCAMIDOPROPYL BETAINE, PEG-7 GLYCERYL COCOATE, PROPYLENE GLYCOL, TETRASODIUM EDTA, PHENOXYETHANOL, SODIUM BENZOATE, LACTIC ACID

Other information

SPL UNCLASSIFIED SECTION

Store at room temperature.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1020365benzalkonium chloride 0.13 % Topical FoamPSN1
1020365benzalkonium chloride 1.3 MG/ML Topical FoamSCD1
1020365benzalkonium chloride 0.13 % Topical FoamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
78658-002-012023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-022023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-032023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-042023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-052023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-062023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-072023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-082023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-092023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-102023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f
78658-002-112023-01-30C16284748780-1f386c649-cf5e-0266-e053-dadaa90a7c1a2eab8a7f-69a0-464a-8cfa-f7bde417675f

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78658-002-01WHAT VIRUS1045000 mL in 1 DRUMLIQUID10450001
78658-002-02WHAT VIRUS209000 mL in 1 DRUMLIQUID2090001
78658-002-03WHAT VIRUS19000 mL in 1 DRUMLIQUID190001
78658-002-04WHAT VIRUS3800 mL in 1 DRUMLIQUID38001
78658-002-05WHAT VIRUS946 mL in 1 BOTTLELIQUID9461
78658-002-06WHAT VIRUS473 mL in 1 BOTTLELIQUID4731
78658-002-07WHAT VIRUS236 mL in 1 BOTTLELIQUID2361
78658-002-08WHAT VIRUS118 mL in 1 BOTTLELIQUID1181
78658-002-09WHAT VIRUS103.5 mL in 1 BOTTLELIQUID103.51
78658-002-10WHAT VIRUS100 mL in 1 BOTTLELIQUID1001
78658-002-11WHAT VIRUS30 mL in 1 BOTTLELIQUID301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78658-002WHAT VIRUS (BENZALKONIUM CHLORIDE) LIQUID [CHAMP PRODUCTS, LTD]1Legacy NDC, 11 package rows20210211_2eab8a7f-69a0-464a-8cfa-f7bde417675f.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78658-00278658-002-01, 78658-002-02, 78658-002-03, 78658-002-04, 78658-002-05, 78658-002-06, 78658-002-07, 78658-002-08, 78658-002-09, 78658-002-10, 78658-002-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
PEG-7 GLYCERYL COCOATEVNX7251543IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
EDETATE SODIUMMP1J8420LUIACT
PHENOXYETHANOLHIE492ZZ3TIACT
SODIUM BENZOATEOJ245FE5EUIACT
LACTIC ACID33X04XA5ATIACT
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB

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
baece089-41d8-3876-e053-2a95a90a144c2eab8a7f-69a0-464a-8cfa-f7bde417675f2021-02-09WarningsExact identifier
spl id: baece089-41d8-3876-e053-2a95a90a144c
spl set id: 2eab8a7f-69a0-464a-8cfa-f7bde417675f

Reported adverse events (FAERS/openFDA)#

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