FDA.reportPublic FDA data

DELICARE NON-ALCOHOL HAND SANITIZER

Manufacturer
CWGC LA Inc.
Effective date
2022-01-03
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:19:38

Label at a glance#

ProductDELICARE NON-ALCOHOL HAND SANITIZER
Active ingredientBENZALKONIUM CHLORIDE
Label structure7 sections

Indications and uses

FOR SANITIZING TO REDUCE BACTERIA ON THE SKIN

Dosage and administration

Apply one shot of foaming sanitizer to dry hands. Rub into skin. No rinsing required.

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 SANITIZING TO REDUCE BACTERIA ON THE SKIN

Warnings

WARNINGS SECTION

For external use only

WHEN USING THIS PRODUCT

  • Avoid contact with eyes. In case of eye contact, flush eyes with water.

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.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply one shot of foaming sanitizer to dry hands.
  • Rub into skin.
  • No rinsing required.

Inactive ingredients

INACTIVE INGREDIENT SECTION

WATER, PROPYLENE GLYCOL, COCAMIDOPROPYL BETAINE, COCAMINE OXIDE, DISODIUM EDTA, DMDM HYDANTOIN, TRIETHANOLAMINE, FRAGRANCE, FD&C YELLOW NO. 5, FD&C BLUE NO. 1

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Delicare - Non-alchol sanitizer - 007-56828-DELDelicare - Non-alchol sanitizer - 007-56828-DEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70415-503-012023-12-13C16284748780-10191ceaa-67c5-198a-e063-dbdaa90aec3eCWGC - DELICARE NON-ALCOHOL HAND SANITIZER (70415-503)
70415-503-012023-07-28C16284748780-10191ceaa-67c5-198a-e063-dbdaa90aec3eCWGC - DELICARE NON-ALCOHOL HAND SANITIZER (70415-503)

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
70415-50370415-503-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
COCAMIDOPROPYL BETAINE5OCF3O11KXIACT
COCAMINE OXIDEQWA2IZI6FIIACT
EDETATE DISODIUM7FLD91C86KIACT
DMDM HYDANTOINBYR0546TOWIACT
TROLAMINE9O3K93S3TKIACT
FD&C YELLOW NO. 5I753WB2F1MIACT
FD&C BLUE NO. 1H3R47K3TBDIACT
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
05df979c-9687-55f4-e063-6294a90a1613d4fa36ed-a331-4f47-a038-87085da8aaf72023-09-21WarningsExact identifier
spl set id: d4fa36ed-a331-4f47-a038-87085da8aaf7

Reported adverse events (FAERS/openFDA)#

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