Hand Wash

Product NDC
70616-628
11-digit product format
706160628
Labeler code
70616
Product ID
70616-628_4a05ad2e-8889-fb63-e063-6294a90abf11
Type
HUMAN OTC DRUG
Nonproprietary name
Benzalkonium chloride
Dosage form
LIQUID
Route
TOPICAL
Labeler
Permatex
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2019-12-20
Substance
BENZALKONIUM CHLORIDE
Active strength
1.3 mg/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Hand Wash
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BENZALKONIUM CHLORIDE1.3 mg/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F5UM2KM3W7Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046593Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
cfd3279e-9584-49d7-bf4b-6ef00d501d9bAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70616-628-96Hand Wash221 mL in 1 BOTTLE, PUMPLIQUID2215

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70616-628HAND WASH (BENZALKONIUM CHLORIDE) LIQUID [PERMATEX]4Current NDC, Legacy NDC, 1 package rows20250305_cfd3279e-9584-49d7-bf4b-6ef00d501d9b.zip

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
Hand WashBENZALKONIUM CHLORIDEPermatexcfd3279e-9584-49d7-bf4b-6ef00d501d9b2026-02-04Warnings, Adverse reactionsExact identifier
ndc (product): 70616-628

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSNcfd3279e-9584-49d7-bf4b-6ef00d501d9b5
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCDcfd3279e-9584-49d7-bf4b-6ef00d501d9b5
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSYcfd3279e-9584-49d7-bf4b-6ef00d501d9b5
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSYcfd3279e-9584-49d7-bf4b-6ef00d501d9b5

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70616-628-9670616062896221 mL in 1 BOTTLE, PUMP (70616-628-96) 221 ml2019-12-200000-00-00NoNoCurrent