Anvi

Manufacturer
Anvi LLC
Effective date
2020-11-17
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-05-31 23:33:52

Label at a glance#

ProductAnvi
Active ingredientBENZALKONIUM CHLORIDE
Label structure13 sections

Dosage and administration

Directions: Dispense an adequate amount into palm to cover hands. Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product. Other Information: Skin cells may shed naturally or by abrasion prior to four hours, exposing fresh, unprotected skin. Reapply as needed.

Storage and handling

Other Information: Skin cells may shed naturally or by abrasion prior to four hours, exposing fresh, unprotected skin. Reapply as needed.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Benzalkonium Chloride .13%..... Antiseptic

Purpose

OTC - PURPOSE SECTION

Antiseptic, Hand Sanitizer

Use(s)

INDICATIONS & USAGE SECTION

Hand and skin sanitizer to decrease microbes on the skin. For use when hand washing is not available.

Warnings

WARNINGS SECTION

For external use only. Keep out of ears, eyes or mouth. In case of contact with eyes, flush with water.

Stop use and ask doctor: If redness or irritation develops and persists for more than 72 hours.

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

Do not use

OTC - DO NOT USE SECTION

Stop use and ask a doctor: If redenss or irritation develops and persists for more than 72 hours.

Directions

OTC - WHEN USING SECTION

Directions: Dispense an adequate amount into palm to cover hands. Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product.

Other Information: Skin cells may shed naturally or by abrasion prior to four hours, exposing fresh, unprotected skin. Reapply as needed.

Stop Use and ask a doctor

OTC - STOP USE SECTION

Stop use and ask a doctor: If redness or irritation develops and persists for more than 72 hours.

Keep out of Reach of Children

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: Dispense an adequate amount into palm to cover hands. Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product.

Directions for Use

DOSAGE & ADMINISTRATION SECTION

Directions: Dispense an adequate amount into palm to cover hands. Rub hands together to cover skin thoroughly until dry. Supervise young children while using this product.

Other Information: Skin cells may shed naturally or by abrasion prior to four hours, exposing fresh, unprotected skin. Reapply as needed.

Other information

STORAGE AND HANDLING SECTION

Other Information: Skin cells may shed naturally or by abrasion prior to four hours, exposing fresh, unprotected skin. Reapply as needed.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water. Colloidal Silicon Dioxide

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

59.15 ml59.15 ml2 oz (59.14 mL) NDC 80201-100-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1049254benzalkonium chloride 0.13 % Topical SolutionPSN4
1049254benzalkonium chloride 1.3 MG/ML Topical SolutionSCD4
1049254benzalkonium chloride 0.13 % Topical SolutionSY4

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80201-200-01Anvi59 mL in 1 BOTTLE, SPRAYLIQUID594
80201-200-02Anvi108 mL in 1 BOTTLE, PUMPLIQUID1084
80201-200-03Anvi167 mL in 1 BOTTLE, PUMPLIQUID1674
80201-200-04Anvi237 mL in 1 BOTTLE, PUMPLIQUID2374
80201-200-05Anvi473 mL in 1 BOTTLE, PUMPLIQUID4734
80201-200-06Anvi946 mL in 1 BOTTLE, PUMPLIQUID9464
80201-200-07Anvi3785 mL in 1 BOTTLE, PUMPLIQUID37854
80201-200-08Anvi18925 mL in 1 PAILLIQUID189254
80201-200-09Anvi208173 mL in 1 DRUMLIQUID2081734
80201-200-10Anvi1040864 mL in 1 CONTAINERLIQUID10408644
80201-200-21Anvi50 mL in 1 BOTTLE, PUMPLIQUID504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80201-200ANVI (BENZALKONIUM CHLORIDE) LIQUID [ANVI LLC]4Legacy NDC, 11 package rows20201119_acb094a4-fda8-56c5-e053-2a95a90a6a25.zip

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 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
b454ed07-49d4-2aab-e053-2995a90a2b56acb094a4-fda8-56c5-e053-2a95a90a6a252020-11-17WarningsExact identifier
spl id: b454ed07-49d4-2aab-e053-2995a90a2b56
spl set id: acb094a4-fda8-56c5-e053-2a95a90a6a25

Reported adverse events (FAERS/openFDA)#

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