Bodycology

Manufacturer: Landy International | Wal-Mart Stores, Inc.
Effective date: 2010-06-24
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: full-release
Hydrated at: 2026-05-31 22:24:55

Label at a glance#

ProductBodycology Brown Sugar Vanilla

Active ingredientTRICLOSAN

Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Purpose

Triclosan 0.30% Antiseptic

WARNINGS SECTION

Warnings:

-For external use only.

-Discontinue use and consult a health care practitioner if irritation develops

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

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

INDICATIONS & USAGE SECTION

Uses: for personal hand hygiene to help prevent the spread of certain bacteria.

Directions: wet hands, apply palmful to hands, scrub thoroughly for 30 seconds, rinse.

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Sodium Laureth Sulfate, Glycerin, Cocamide DEA, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Alcohol Denat., Propylene Glycol, Fragrance (Parfum), Triethanolamine, Polyethylene, Disodium EDTA, Aloe Barbadensis (Aloe Vera) Leaf Juice, Tocopheryl Acetate, Butyrospermum Parkii (Shea Butter), Benzophenone-4, Methylchloroisothiazolinone, Methylisothiazolinone. May Contain: Ultramarines (CI 77007), Yellow 5 (CI 19140), Yellow 6 (CI 15985), Yellow 10 (CI 47005), Red 33 (CI 17200), Red 4 (CI 14700), Red 40 (CI 16035), Blue 1 (CI 42090)

image of back label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Anti-Bacterial Scrubbing Hand Soap
177 ml/6 fl oz.

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
260054	triclosan 0.3 % Medicated Liquid Soap	PSN	3
260054	triclosan 3 MG/ML Medicated Liquid Soap	SCD	3
260054	triclosan 0.3 % Foaming Medicated Hand Soap	SY	3
260054	triclosan 0.3 % Medicated Liquid Soap	SY	3

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51706-113-02	2019-10-21	C162847	48780-1	956f9ecf-ded5-621f-e053-dbdaa90a74ad	Brown Sugar Vanilla

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
51706-113-01	BodycologyBrown Sugar Vanilla	177 mL in 1 BOTTLE	GEL	177		3
51706-113-02	BodycologyBrown Sugar Vanilla	1 in 1 KIT	GEL	1		3

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51706-113	BODYCOLOGY BROWN SUGAR VANILLA (TRICLOSAN) GEL [LANDY INTERNATIONAL]	3	Legacy NDC, 2 package rows	20100625_d2aaa375-1fa8-4172-b472-e77a08a0844b.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version	Uploaded
TRICLOSAN	ACTIVE INGREDIENT	4NM5039Y5X	3
TRICLOSAN	ACTIVE MOIETY	4NM5039Y5X	3

Products#

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

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

Bodycology Brown Sugar Vanilla
Triclosan

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
51706-113	51706-113-01, 51706-113-02

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
Name	UNII	Kind
TRICLOSAN	4NM5039Y5X	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
9bb371f4-f52a-4483-a20a-f64993c887d6			d2aaa375-1fa8-4172-b472-e77a08a0844b	2010-06-24	Warnings	Exact identifier spl id: 9bb371f4-f52a-4483-a20a-f64993c887d6 spl set id: d2aaa375-1fa8-4172-b472-e77a08a0844b

Reported adverse events (FAERS/openFDA)#

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