FDA.reportPublic FDA data

Soft Wet Wipes

Manufacturer
Rite-Kem Incorporated
Effective date
2023-01-10
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:41:11

Label at a glance#

ProductSoft Wet Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure11 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium chloride 0.13%

OTC - PURPOSE SECTION

Antiseptic

INDICATIONS & USAGE SECTION

Hand Sanitizing Wipe to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

WARNINGS SECTION

For external use only.

OTC - DO NOT USE SECTION

  • In children less than 2 months of age
  • on open skin wounds
  • If you are allergic to any of the ingredients

OTC - STOP USE SECTION

Discontinue use if irritiation or redness develops. If conditions persist for more than 2 hours consult a physician.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children unless under adult supervision. If swallowed, get medical help or contact a poison control center immediately.

DOSAGE & ADMINISTRATION SECTION

Directions for Use:

  • Thoroughly wipe hands with wipe.
  • Discard in trash receptacle.
  • Do not flush.
  • Be sure to reseal label completely to retain moisture.

OTHER SAFETY INFORMATION

Other information

store between 15-30 c (59-86F)

Avoid freezing and excessing heat above 40 c (104F)

INACTIVE INGREDIENT SECTION

Inactive ingredients: Water, Propylene Glycol, Disodium EDTA, Chloromethylisothlazolinone, Methylisothiazolinone, Potassium Sorbate, Quaternium-15, Aloe Barbadansis Leaf Juice, Disodium Cocoamphodiacetate, Tocopheryl Acetate, Polysorbate-20, Citric Acid, Fragrance.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Soft Wet Wipes

(15 Count)

See Back Panel for Use Information

RITE-KEM

Sold by Rite-Kem Inc. T

703 Westmoreland Tupelo MS 38801

www.RITE-KEM.com

NDC: 73943-950-01

Front PanelFront Panel

Back PanelBack Panel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73943-950-012025-03-21C16284748780-12cef2736-781f-d83d-e063-dadaa90ab31fHand Sanitizer Wipes (BZK) - Soft Wet Wipes
73943-950-012025-01-30C16284748780-12cef2736-781f-d83d-e063-dadaa90ab31fHand Sanitizer Wipes (BZK) - Soft Wet Wipes

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73943-95073943-950-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
WATER059QF0KO0RIACT
CITRAL PROPYLENE GLYCOL ACETAL9W7YHX7EX6IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
ALOEV5VD430YW9IACT
DISODIUM COCOAMPHODIACETATE18L9G3U51MIACT
QUATERNIUM-15E40U03LEM0IACT
FRAGRANCE CLEAN ORC0600327329LCV5BTFIACT
MAGNESIUM DISODIUM EDTANDT563S5VZIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
METHYLCHLOROISOTHIAZOLINONE/METHYLISOTHIAZOLINONE MIXTURE15O9QS218WIACT
POLYSORBATE 207T1F30V5YHIACT
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
30e0d333-9cbe-5143-e063-6294a90a6ab1c24e99b8-0051-74d7-e053-2a95a90a0ce42025-02-12WarningsExact identifier
spl set id: c24e99b8-0051-74d7-e053-2a95a90a0ce4

Reported adverse events (FAERS/openFDA)#

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