DetraPel Hand Sanitizer

Manufacturer
DetraPel, Inc.
Effective date
2020-04-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:34:30

Label at a glance#

ProductDetraPel Hand Sanitizer
Active ingredientBENZALKONIUM CHLORIDE
Label structure8 sections

Indications and uses

For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Spray a small amount of liquid into palm of hand Rub thorougly over all surfaces of both hands Rub hands together briskly until dry

Label contents#

Full prescribing information#

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active IngredientPurpose

Benzalkonium Chloride 0.13% .............

Antimicrobial

Uses

OTC - PURPOSE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

Warnings:

WARNINGS SECTION

For external use only

When using this product avoid contact with eyes. In case of eye contact, flush eyes with water.

Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray a small amount of liquid into palm of hand
  • Rub thorougly over all surfaces of both hands
  • Rub hands together briskly until dry

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, dihyroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, fragrance.

Uses

INDICATIONS & USAGE SECTION

  • For hand sanitizing to decrease bacteria on the skin
  • Recommended for repeated use

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DetraPel Hand Sanitizer

DetraPel Hand SanitizerDetraPel Hand Sanitizer

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
74961-2300-22023-04-10C16284748780-1d6a99b39-3ae6-a426-e053-dadaa90af4c2a3801620-f99b-2e39-e053-2a95a90a3b45
74961-2300-22022-01-28C16284748780-1d6a99b39-3ae6-a426-e053-dadaa90af4c2a3801620-f99b-2e39-e053-2a95a90a3b45

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
74961-230074961-2300-2
71023-445

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
f9013f9e-e6a6-b618-e053-6294a90ab191a3801620-f99b-2e39-e053-2a95a90a3b452023-04-10WarningsExact identifier
spl set id: a3801620-f99b-2e39-e053-2a95a90a3b45

Reported adverse events (FAERS/openFDA)#

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