71141-021-02, LIDL US LLC

Manufacturer
LIDL US LLC | Apollo Health and Beauty Care
Effective date
2026-05-20
Label type
HUMAN OTC DRUG LABEL
Version
7
Source
full-release
Hydrated at
2026-06-01 01:58:43

Label at a glance#

ProductLIDL
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

For Hand washing to decrease bacteria on the skin

Dosage and administration

Apply onto dry hands Lather and rinse thoroughly with water.

Label contents#

Full prescribing information#

Active Ingredient.

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride (0.13%)

Purpose

OTC - PURPOSE SECTION

Antibacterial

Uses

INDICATIONS & USAGE SECTION

  • For Hand washing to decrease bacteria on the skin

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

Avoid contact with eyes. In case of contact, rinse thoroughly with water.

Stop use and ask a doctor

OTC - STOP USE SECTION

If irritation or redness develops and lasts 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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply onto dry hands
  • Lather and rinse thoroughly with water.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Cocamidopropyl Betaine, Polysorbate 20, Fragrance (Parfum), Glycerin, Decyl Glucoside, Hydroxyethylcellulose, Aloe Barbadensis Leaf Juice, Camellia Sinensis Leaf Extract, Polyquatermium-7, Propylene Glycol, Tetrasodium EDTA, Sodium Citrate, Citric Acid, Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone, Blue 1 (Cl 42090), Red 33 (CI 17200).

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LIDL FRSH WTR AB 12X7.5OZ FHSPLIDL FRSH WTR AB 12X7.5OZ FHSP

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapPSN7
1046593benzalkonium chloride 1.3 MG/ML Medicated Liquid SoapSCD7
1046593benzalkonium chloride 0.13 % Medicated Liquid SoapSY7
1046593benzalkonium chloride 1.33 MG/ML Medicated Liquid SoapSY7

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-820738372GTIN-8: 20738372
EAN-8: 20738372
GTIN storage (14 digits): 00000020738372
ca13c2e3-2927-ec44-e053-2995a90adfb4.jpg, LIDL FRSH WTR AB 12X7.5OZ FHSP.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71141-021-02LIDL222 mL in 1 BOTTLE, PLASTICSOAP2227

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71141-02171141-021-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
62026-05-03weekly-update2026-06-03 18:02:43

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
LIDLBENZALKONIUM CHLORIDELIDL US LLCca13681e-4cdd-30c7-e053-2a95a90ad05a2026-05-20WarningsExact identifier
ndc (package): 71141-021-02
ndc (product): 71141-021
ndc11 (package): 71141002102
spl id: 52413030-c6ef-994d-e063-6394a90ad499
spl set id: ca13681e-4cdd-30c7-e053-2a95a90ad05a

Reported adverse events (FAERS/openFDA)#

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