FDA.reportPublic FDA data

Vanish

Manufacturer
Tinks | Albaad USA, Inc.
Effective date
2010-07-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:26:11

Label at a glance#

ProductVanish
Active ingredientBenzalkonium Chloride
Label structure7 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient

Benzalkonium Chloride 0.13%

OTC - PURPOSE SECTION

Purpose

Antimicrobial

INDICATIONS & USAGE SECTION

Uses

For hand sanitizing to decrease bacteria on the skin

Recommended for repeated use

WARNINGS SECTION

Warnings

For external use only

OTC - WHEN USING SECTION

When using this product avoid contact with eyes.

In case of eye contact, flush eyes with water.

OTC - STOP USE SECTION

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

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.

DOSAGE & ADMINISTRATION SECTION

Directions

Apply to skin as desired.

Allow to dry without wiping.

INACTIVE INGREDIENT SECTION

Inactive Ingredients

water, dihydroxypropyl PEG-5 linoleammonium chloride, glycereth-2 cocoate, behentrimonium chloride, dihydroxyethyl cocamine oxide, polyaminopropyl biguanide, dimethicone, C12-15 pareth-7, alkyl polyglucoside

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

No Hype

Just Science

Tinks

Vanish

Hunting

Odor Eliminating Field Wipes

Patented Byotrol Technology

Alcohol and Scent Free

Wont dry skin - moisturizes while it sanitizes

Kills 99.99% of germs that cause odor and illness

(after a 15 second wet time)

Durable 6.7" by 7.9" Size

20 count re-sealable pack

tinks69.com

Net Weight: 4.5 oz (128g)

Safe and Strong enough for use in Medical and Food Industries

Science Fact, Not Science Fiction

container labelcontainer label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN1
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD1
1049254benzalkonium chloride 0.13 % Topical SolutionSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52473-001-012020-01-31C16284748780-19d75b9d0-effb-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52473-001-01Vanish83.5 mL in 1 POUCHLIQUID83.51

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52473-001VANISH (BENZALKONIUM CHLORIDE) LIQUID [TINKS]1Legacy NDC, 1 package rows20101021_aab02679-a2d0-43dc-b491-eb822cdca16d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Benzalkonium ChlorideACTIVE INGREDIENTF5UM2KM3W71
BenzalkoniumACTIVE MOIETY7N6JUD5X6Y1
Behentrimonium chlorideINACTIVE INGREDIENTX7GNG3S47T1
Dihydroxyethyl cocamine oxideINACTIVE INGREDIENT8AR51R3BL51
Dihydroxypropyl PEG-5 linoleammonium chlorideINACTIVE INGREDIENT0Y0NQR2GH11
DimethiconeINACTIVE INGREDIENT92RU3N3Y1O1
Glycereth-2 cocoateINACTIVE INGREDIENTJWM00VS7HC1
Polyaminopropyl biguanideINACTIVE INGREDIENT322U039GMF1
WaterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52473-00152473-001-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
Benzalkonium ChlorideF5UM2KM3W7ACTIB
Water059QF0KO0RIACT
Dihydroxypropyl PEG-5 linoleammonium chloride0Y0NQR2GH1IACT
Glycereth-2 cocoateJWM00VS7HCIACT
Behentrimonium chlorideX7GNG3S47TIACT
Dihydroxyethyl cocamine oxide8AR51R3BL5IACT
Polyaminopropyl biguanide322U039GMFIACT
Dimethicone92RU3N3Y1OIACT

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
502d8daf-8b6f-4651-b0ae-08e205bcdf16aab02679-a2d0-43dc-b491-eb822cdca16d2010-07-07WarningsExact identifier
spl id: 502d8daf-8b6f-4651-b0ae-08e205bcdf16
spl set id: aab02679-a2d0-43dc-b491-eb822cdca16d

Reported adverse events (FAERS/openFDA)#

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