Bodycology white gardenia anti-bacterial foaming hand soap

Manufacturer
American Blending and Filling
Effective date
2010-04-20
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:24:29

Label at a glance#

ProductBodycology white gardenia anti-bacterial foaming hand soap
Active ingredientTriclosan
Label structure3 sections

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Triclosan

OTC - PURPOSE SECTION

Purpose  Antiseptic

Uses   For handwashing to decrease bacteria on the skin.

WARNINGS SECTION

Warnings  For external use only

OTC - WHEN USING SECTION

Do not get into eyes.  If contact occurs, rinse eyes throughly with water.

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.

SPL UNCLASSIFIED SECTION

Directions  Wet hands. Apply palmful to hands.  Scrub thoroughly for 30 seconds. Rinse.

INACTIVE INGREDIENT SECTION


Inactive Ingredients
  Water (Aqua, Eau), Sodium Laureth Sulfate, Cocamidopropyl Betaine, Glycereth-26, Glycerine, Fragrance (Parfum), PEG-120 Methyl Glucose Dioleate, PEG-7 Glyceryl Cocoate, Aloe Barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate, Sodium Chloride, Oleth-20, Xanthan Gum, Isopropyl Alcohol, Citric acid, Benzophenone-4, Tetrasodium EDTA, Benzyl Salicylate, Hexyl Cinnamal, Linalool, Methylchloroisothiazolinone, Methylisothaizolinone. May Contain: Ultramarines (Cl 77007), Yellow 5 (Cl 19140), Yellow 6 (CL 15985), Yellow 10 (Cl 47005), Red 33 (Cl 17200), Red 4 (Cl 14700), Red 40 (Cl 16035), Blue 1 (Cl 42090), Green (Cl 42053), Ext. Violet (Cl 60730).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Front LabelFront Label

DESCRIPTION SECTION

Back LabelBack Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
260054triclosan 0.3 % Medicated Liquid SoapPSN1
260054triclosan 3 MG/ML Medicated Liquid SoapSCD1
260054triclosan 0.3 % Foaming Medicated Hand SoapSY1
260054triclosan 0.3 % Medicated Liquid SoapSY1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
65663-020-012019-10-21C16284748780-1956f9ecf-d608-621f-e053-dbdaa90a74adDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
65663-020-01Bodycology white gardenia anti-bacterial foaming hand soap244 mL in 1 BOTTLELIQUID2441

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
65663-020BODYCOLOGY WHITE GARDENIA ANTI-BACTERIAL FOAMING HAND SOAP (TRICLOSAN) LIQUID [AMERICAN BLENDING AND FILLING]1Legacy NDC, 1 package rows20100512_27cb8e40-4706-43df-86c9-3dd0dc88ccf7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
TriclosanACTIVE INGREDIENT4NM5039Y5X1
TriclosanACTIVE MOIETY4NM5039Y5X1

Products#

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

DailyMed product names page 1 of 1 · 2 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
65663-02065663-020-01

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Triclosan4NM5039Y5XACTIB

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
e6185362-4152-4722-95c6-0dc6903027de27cb8e40-4706-43df-86c9-3dd0dc88ccf72010-04-20WarningsExact identifier
spl id: e6185362-4152-4722-95c6-0dc6903027de
spl set id: 27cb8e40-4706-43df-86c9-3dd0dc88ccf7

Reported adverse events (FAERS/openFDA)#

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