FDA.reportPublic FDA data

ALCOHOL HAND SANITIZER

Manufacturer
CWGC LA Inc.
Effective date
2022-01-03
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:36

Label at a glance#

ProductALCOHOL HAND SANITIZER
Active ingredientALCOHOL
Label structure8 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

Ethyl Alcohol 70 %

PURPOSE

OTC - PURPOSE SECTION

ANTIBACTERIAL

Uses

INDICATIONS & USAGE SECTION

  • FOR SANITIZING TO REDUCE BACTERIA ON THE SKIN.

Warnings

WARNINGS SECTION

FOR EXTERNAL USE ONLY

FLAMMABLE : KEEP AWAY FROM FIRE OR FLAME

WHEN USING THIS PRODUCT

  • AVOID CONTACT WITH EYES, IN CASE OF EYE CONTACT, FLUSH 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, ISOPROPYL ALCOHOL, PROPYLENE GLYCOL, PEG-12 DIMETHICONE CROSSPOLYMER, BIS-PEG-12 DIMETHICONE

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Delicare_Alcohol Hand Sanitizer_1000mL01b LBL_Delicare_Alcohol Hand Sanitizer_1000mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70415-601-112023-12-13C16284748780-10191ceaa-67fe-198a-e063-dbdaa90aec3eCWGC - Delicare Alcohol Hand Sanitizer 70% Ethyl Alcohol (70415-601)
70415-601-112023-07-28C16284748780-10191ceaa-67fe-198a-e063-dbdaa90aec3eCWGC - Delicare Alcohol Hand Sanitizer 70% Ethyl Alcohol (70415-601)

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
70415-60170415-601-11

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
ISOPROPYL ALCOHOLND2M416302IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
PEG-12 DIMETHICONE (300 CST)ZEL54N6W95IACT
BIS-PEG-12 DIMETHICONE (70 MPA.S)2JDK5W22H4IACT
ALCOHOL3K9958V90MACTIB

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
05dfa030-a4ea-13c3-e063-6394a90a8f74b8735594-5437-40cf-a552-bcddc94a9c802023-09-21WarningsExact identifier
spl set id: b8735594-5437-40cf-a552-bcddc94a9c80

Reported adverse events (FAERS/openFDA)#

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