FDA.reportPublic FDA data

PRO-LINK Foaming Antimicrobial So ap

Manufacturer
Pro-Link, Inc.
Effective date
2020-12-23
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:00:08

Label at a glance#

ProductPRO-LINK Foaming Antimicrobial So ap
Active ingredientCHLOROXYLENOL
Label structure7 sections

Indications and uses

Handwash to help decrease bacteria on the skin Recommended for repeated use

Dosage and administration

Wet hands Apply a small amount of product and work into a lather Rinse well and dry hands completely

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol 0.3%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Uses

INDICATIONS & USAGE SECTION

  • Handwash to help decrease bacteria on the skin
  • Recommended for repeated use

Warnings

WARNINGS SECTION

For external use only

OTC - WHEN USING SECTION

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

OTC - STOP USE SECTION

Stop use and ask a doctor if irritation or rash appears and lasts

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

  • Wet hands
  • Apply a small amount of product and work into a lather
  • Rinse well and dry hands completely

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Product LabelProduct Label

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
66908-08266908-082-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
CHLOROXYLENOL0F32U78V2QACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT
AMMONIUM LAURETH-2 SULFATE698O4Z48G6IACT
AMMONIUM LAURYL SULFATEQ7AO2R1M0BIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
AMMONIUM XYLENESULFONATE4FZY6L6XCMIACT
COCO MONOETHANOLAMIDEC80684146DIACT
GLYCERINPDC6A3C0OXIACT
ISOPROPYL ALCOHOLND2M416302IACT
LACTIC ACID33X04XA5ATIACT
VITAMIN A PALMITATE1D1K0N0VVCIACT
JOJOBA OIL724GKU717MIACT
EDETATE SODIUMMP1J8420LUIACT
.ALPHA.-TOCOPHEROL ACETATE, D-A7E6112E4NIACT
CORN OIL8470G57WFMIACT
AMMONIUM SULFATESU46BAM238IACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
FD&C RED NO. 4X3W0AM1JLXIACT
FD&C YELLOW NO. 6H77VEI93A8IACT

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
53092fb7-f8f4-4996-8731-5a25e60574173910286f-7856-4cfd-bbf6-b511b3c54efc2020-12-23WarningsExact identifier
spl id: 53092fb7-f8f4-4996-8731-5a25e6057417
spl set id: 3910286f-7856-4cfd-bbf6-b511b3c54efc

Reported adverse events (FAERS/openFDA)#

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