FDA.reportPublic FDA data

DRUMMOND AMERICAN TRADE WIND Antimicrobial Lotion Soap

Manufacturer
Lawson Products, Inc. | Canberra Corporation
Effective date
2010-08-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:31

Label at a glance#

ProductDrummond American Trade Wind Antimicrobial
Active ingredientchloroxylenol
Label structure9 sections

Indications and uses

Helps reduce bacteria that potentially can cause disease Helps prevent cross contamination by hand contact

Dosage and administration

Wet hands and forearms Apply appropriate amount to palm and hand Scrub hands and forearms for 60 seconds Rinse well Wipe dry with towel, repeat if necessary.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Chloroxylenol (1% v/v)

Purpose

OTC - PURPOSE SECTION

Antiseptic Hand Sanitizer

Uses

INDICATIONS & USAGE SECTION

  • Helps reduce bacteria that potentially can cause disease
  • Helps prevent cross contamination by hand contact

Warnings

WARNINGS SECTION

  • For external use only
  • Do not use near eyes
  • Keep out of reach of children.
  • In case of eye contact flush with water for 15 minutes
  • If irritation persists, get medical attention
  • In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wet hands and forearms
  • Apply appropriate amount to palm and hand
  • Scrub hands and forearms for 60 seconds
  • Rinse well
  • Wipe dry with towel, repeat if necessary.

Other Information

SPL UNCLASSIFIED SECTION

  • Assists with OSHA bloodborne pathogen standard compliance

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Cocoate, Oleate, Cocamidopropyl betaine, Hydroxyethyl Cellulose, Polyquaternium 7, Na4EDTA, 2-Propanol, Peg-75 Lanolin, Aloe Vera Gel, Fragrance, Triclosan, DMDM Hydantoin.

Principal Display Panel – Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DRUMMOND AMERICAN

TRADE WIND

Antimicrobial Lotion Soap

KEEP OUT OF REACH OF CHILDREN

SEE DRUG FACTS PANEL FOR ADDITIONAL INFORMATION.

©Drummond American Corporation 1995 Reproduction in whole or in part prohibited DL3070-0505

Made & printed in U.S.A.

Figure
Figure

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
413257chloroxylenol 1 % Medicated Liquid SoapPSN1
413257chloroxylenol 10 MG/ML Medicated Liquid SoapSCD1
413257chloroxylenol 1 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62428-505-552019-10-21C16284748780-1956f9ecf-c69f-621f-e053-dbdaa90a74adDRUMMOND AMERICAN TRADE WIND Antimicrobial Lotion Soap

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62428-505-55Drummond American Trade Wind Antimicrobial3785 mL in 1 BOTTLELIQUID37851

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62428-505DRUMMOND AMERICAN TRADE WIND ANTIMICROBIAL (CHLOROXYLENOL) LIQUID [LAWSON PRODUCTS, INC.]1Legacy NDC, 1 package rows20100811_bf78b388-3d6a-4b5d-9307-61e98bc1594e.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
chloroxylenolACTIVE INGREDIENT0F32U78V2Q1
chloroxylenolACTIVE MOIETY0F32U78V2Q1
aloe vera leafINACTIVE INGREDIENTZY81Z83H0X1
cocamidopropyl betaineINACTIVE INGREDIENT5OCF3O11KX1
DMDM hydantoinINACTIVE INGREDIENTBYR0546TOW1
edetate sodiumINACTIVE INGREDIENTMP1J8420LU1
hydroxyethyl cellulose (2000 CPS at 1%)INACTIVE INGREDIENTS38J6RZN161
isopropyl alcoholINACTIVE INGREDIENTND2M4163021
polyquaternium-7 (70/30 acrylamide/DADMAC; 1600 kd)INACTIVE INGREDIENT0L414VCS5Y1
potassium cocoateINACTIVE INGREDIENTF8U72V8ZXP1
potassium oleateINACTIVE INGREDIENT74WHF607EU1
triclosanINACTIVE INGREDIENT4NM5039Y5X1
waterINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62428-50562428-505-55

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
chloroxylenol0F32U78V2QACTIB
water059QF0KO0RIACT
potassium oleate74WHF607EUIACT
cocamidopropyl betaine5OCF3O11KXIACT
hydroxyethyl cellulose (2000 CPS at 1%)S38J6RZN16IACT
isopropyl alcoholND2M416302IACT
edetate sodiumMP1J8420LUIACT
aloe vera leafZY81Z83H0XIACT
DMDM hydantoinBYR0546TOWIACT
triclosan4NM5039Y5XIACT
potassium cocoateF8U72V8ZXPIACT
polyquaternium-7 (70/30 acrylamide/DADMAC; 1600 kd)0L414VCS5YIACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 38 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
edetate sodiumEDETATE SODIUMMP1J8420LUSPONGE / TOPICAL0.14 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
polyquaternium-7 (70/30 acrylamide/DADMAC; 1600 kd)POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW)0L414VCS5YSHAMPOO / TOPICAL1 %w/wExact identifier — unii candidate
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SYRUP / ORAL2 mg/5mlExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16POWDER, FOR SUSPENSION / ORAL560 mgExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LULOTION / TOPICAL0.17 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16LOTION / TOPICAL0.2 %w/vExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUSHAMPOO / TOPICAL1.33 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUSOLUTION / TOPICAL0.3 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUSOAP / TOPICAL0.12 %w/wExact identifier — unii candidate
12 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SUSPENSION / OPHTHALMIC0.25 %w/vExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUTABLET / ORAL5 mgExact identifier — unii candidate
12 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302SWAB / TOPICAL43.9 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16TABLET, CHEWABLE / ORAL5.9 mgExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION/ DROPS / OPHTHALMIC0.5 %w/vExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SUSPENSION / ORAL100 mgExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUSOLUTION / OPHTHALMIC0.1 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUINJECTION / INTRAVENOUS0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302GEL / TOPICAL75 mgExact identifier — unii candidate
9 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302GEL, METERED / TOPICAL525 mgExact identifier — unii candidate
9 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302OIL / TOPICAL72 mgExact identifier — unii candidate
9 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUCAPSULE / ORAL1 mgExact identifier — unii candidate
12 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302OIL / AURICULAR (OTIC)6 mgExact identifier — unii candidate
9 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SPRAY / NASAL0.1 mg/0.2mlExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUEMULSION / OPHTHALMIC0.02 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SUSPENSION / TOPICAL0.69 %w/vExact identifier — unii candidate
15 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302SPONGE / TOPICAL4 %w/wExact identifier — unii candidate
9 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16GEL / TOPICAL4 mgExact identifier — unii candidate
15 equally ranked IID candidates
DMDM hydantoinDMDM HYDANTOINBYR0546TOWLOTION / TOPICAL3 mgExact identifier — unii candidate
isopropyl alcoholISOPROPYL ALCOHOLND2M416302TABLET, EXTENDED RELEASE / ORALNAExact identifier — unii candidate
9 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302SOLUTION / TOPICAL40 %w/vExact identifier — unii candidate
9 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUINJECTION / INTRAMUSCULAR0.01 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
isopropyl alcoholISOPROPYL ALCOHOLND2M416302LOTION, AUGMENTED / TOPICAL2070 mgExact identifier — unii candidate
9 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SUSPENSION / AURICULAR (OTIC)1 mgExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION / ORAL3 mgExact identifier — unii candidate
15 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16TABLET, EXTENDED RELEASE / ORAL350 mgExact identifier — unii candidate
15 equally ranked IID candidates
edetate sodiumEDETATE SODIUMMP1J8420LUINJECTION, SOLUTION / INTRAVENOUS0.04 %w/vExact identifier — unii candidate
12 equally ranked IID candidates
hydroxyethyl cellulose (2000 CPS at 1%)HYDROXYETHYL CELLULOSE (2000 MPA.S AT 1%)S38J6RZN16SOLUTION / TOPICAL0.21 %w/vExact identifier — unii candidate
15 equally ranked IID candidates

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
4ce03b23-3b02-41b0-ab8d-148a5e4dd5f4bf78b388-3d6a-4b5d-9307-61e98bc1594e2010-08-01WarningsExact identifier
spl id: 4ce03b23-3b02-41b0-ab8d-148a5e4dd5f4
spl set id: bf78b388-3d6a-4b5d-9307-61e98bc1594e

Reported adverse events (FAERS/openFDA)#

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