Advanced Alcohol Gel Sanitizer III

Manufacturer
Betco Corporation LTD | ZHEJIANG RIFESHOW COSMETICS CO.,LTD
Effective date
2020-05-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:31:11

Label at a glance#

ProductAdvanced Alcohol Gel Sanitizer III
Active ingredientALCOHOL
Label structure8 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Antimicrobial

OTC - ACTIVE INGREDIENT SECTION

Alcohol

INDICATIONS & USAGE SECTION

• Hand sanitizer to reduce microorganisms on the skin.
• Use this product when soap and water are not available.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of children

WARNINGS SECTION

For external use only. • Avoid contact with eyes. If contact occurs, rinse thoroughly with water. • FLAMMABLE. This product contains ethyl alcohol. Keep away from sources of ignition. • Discontinue use if irritation or redness develops. • If irritation persists for more than 72 hours, consult a physician. • If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

• Place enough product on your palm to thoroughly cover your hands.
• Rub hands together briskly for 30 seconds until dry.

INACTIVE INGREDIENT SECTION

Deionized Water, Glycerin, Carbomer, Triethanolamine.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

65601-009-8865601-009-88

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65601-009-882024-11-21C16284748780-10191ceaa-6e69-198a-e063-dbdaa90aec3eAdvanced Alochol Gel Sanitizer III
65601-009-882023-07-28C16284748780-10191ceaa-6e69-198a-e063-dbdaa90aec3eAdvanced Alochol Gel Sanitizer III

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65601-00965601-009-88

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML · Source PDF

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
275bb642-3447-b2b1-e063-6294a90af281a57604b4-488f-327c-e053-2995a90ac1ab2024-11-20WarningsExact identifier
spl set id: a57604b4-488f-327c-e053-2995a90ac1ab

Reported adverse events (FAERS/openFDA)#

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