FDA.reportPublic FDA data

Diamond Wipes Antibacterial Hand Wipes

Manufacturer
Diamond Wipes International, Inc.
Effective date
2020-02-25
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:40:15

Label at a glance#

ProductDiamond Wipes Antibacterial Hand Wipes
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Dosage and administration

For hand washing to decrease bacteria on skin reccomended for repeated use

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride 0.13%

Purpose

OTC - PURPOSE SECTION

Antibacterial

Directions

INDICATIONS & USAGE SECTION

  • For hand washing to decrease bacteria on skin
  • reccomended for repeated use

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

avoid contact with eyes

Stop use and ask a doctor 

OTC - STOP USE SECTION

   If irritation or redness 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

Directions

DOSAGE & ADMINISTRATION SECTION

  • open packet
  • remove and unfold wipes
  • wipe hands thoroughly for approximately 15 seconds
  • do not flush

Inactive ingredients

INACTIVE INGREDIENT SECTION

Alcohol Denat., Aloe Barbadensis Leaf Juice, Citric Acid, Fragrance, Polysorbate 20, Sorbic Acid, Tocopheryl Acetate, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

  • Diamond Wipes
  • Antibacterial Hand Wipes
  • Kills 99% of Germs
  • Aloe vera and Vitamin E
  • Made in USA

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
64709-101-102024-05-09C16284748780-1d6a99b39-8754-a426-e053-dadaa90af4c2Diamond Wipes Antibacterial Hand Wipes
64709-101-102022-01-28C16284748780-1d6a99b39-8754-a426-e053-dadaa90af4c2Diamond Wipes Antibacterial Hand Wipes

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
64709-10164709-101-10

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
BENZALKONIUM CHLORIDEF5UM2KM3W7ACTIB
POLYSORBATE 207T1F30V5YHIACT
Sorbic acidX045WJ989BIACT
GLYCERINPDC6A3C0OXIACT
ALCOHOL3K9958V90MIACT
water059QF0KO0RIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
.ALPHA.-TOCOPHEROL ACETATE, DL-WR1WPI7EW8IACT
ALOE VERA LEAFZY81Z83H0XIACT

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
44fd46d8-358b-1908-e063-6294a90ad6f6b126d10a-256f-4ed2-af83-792bbcaa57a32025-12-02WarningsExact identifier
spl set id: b126d10a-256f-4ed2-af83-792bbcaa57a3

Reported adverse events (FAERS/openFDA)#

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