60 soft wipes

Manufacturer
SHANGHAI SANJUN GENERAL MERCHANDISE CO., LTD.
Effective date
2022-12-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:52:24

Label at a glance#

Product60 soft wipes
Active ingredientDIDECYLDIMONIUM CHLORIDE, BENZALKONIUM CHLORIDE
Label structure6 sections

Dosage and administration

Storage. Store at room temperature. Dispensing. Remove seal band. Lift tab at front of lid. Pull up corner of center sheet and thread through dispenser slit in lid. Close lid to retain moisture. Use. Apply wipe thoroughly to hands as desired. Allow to dry without wiping. Disposal. Dispose of used wipes in trash receptacle after use. Do not flush.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.1 %

Didecyldimonium Chloride 0.15%

OTC - PURPOSE SECTION

Antiseptic

USE

INDICATIONS & USAGE SECTION

For hand sanitizing to decrease bacteria on the skin.

Warning

WARNINGS SECTION

For external use only.
Do not use
In the eyes.
If you are allergic to any of these ingredients.
Stop use and ask a doctor if irritation and redness develop and persist for more than 72 hours.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Storage. Store at room temperature.
Dispensing. Remove seal band. Lift tab at front of lid. Pull up corner of center sheet and thread through dispenser slit in lid. Close lid to retain moisture.
Use. Apply wipe thoroughly to hands as desired. Allow to dry without wiping.
Disposal. Dispose of used wipes in trash receptacle after use. Do not flush.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Purified Water, Propylene Glycol, Glycerin, Ethylhexylglycerin, Bronopol, Aloe Barbadensis Leaf Extract, Tocopherol Acetate.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1111

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
75670-011-012025-01-30C16284748780-12cef2736-6763-d83d-e063-dadaa90ab31f75670-011 60 soft wipes Benzalkonium Chloride 0.1% Didecyldimonium Chloride 0.15%

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
75670-011-0160 soft wipes48 in 1 CARTONCLOTH481
75670-011-0160 soft wipes60 in 1 PAILCLOTH601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
75670-01160 SOFT WIPES (BENZALKONIUM CHLORIDE) CLOTH [SHANGHAI SANJUN GENERAL MERCHANDISE CO., LTD.]1Legacy NDC, 2 package rows20221212_ef869dea-50d4-be48-e053-2995a90a78c7.zip

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
75670-01175670-011-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 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
ef869dea-50d5-be48-e053-2995a90a78c7ef869dea-50d4-be48-e053-2995a90a78c72022-12-10WarningsExact identifier
spl id: ef869dea-50d5-be48-e053-2995a90a78c7
spl set id: ef869dea-50d4-be48-e053-2995a90a78c7

Reported adverse events (FAERS/openFDA)#

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