Bodycology

Manufacturer
Landy International | Wal-Mart Stores, Inc.
Effective date
2010-07-07
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 22:25:05

Label at a glance#

ProductBodycology Brown Sugar Vanilla Hand Sanitizer
Active ingredientALCOHOL
Label structure2 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient  

Ethyl Alcohol 65%

WARNINGS SECTION

Warnings: For external use only. When using this product 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: to decrease bacteria on the skin that could cause disease.

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water (Aqua), Isopropyl Myristate, Propylene Glycol, Triethanolamine, Carbomer, Fragrance (Parfum), Aloe Barbadensis (Aloe Vera) Leaf Juice, Yellow 5 (CI 19140), Ext. Violet 2 (CI 60730)

image of back labelimage of back label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Cherry Blossom Hand Sanitizer

30 mL 1 FL OZ

image of front labelimage of front label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51706-202-022019-10-21C16284748780-1956f9ecf-d980-621f-e053-dbdaa90a74adBrown Sugar Vanilla Hand Sanitizer

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51706-202-01Bodycology Brown Sugar Vanilla Hand Sanitizer30 mL in 1 BOTTLEGEL301
51706-202-02Bodycology Brown Sugar Vanilla Hand Sanitizer1 in 1 BOXGEL11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51706-202BODYCOLOGY BROWN SUGAR VANILLA HAND SANITIZER (ETHYL ALCOHOL) GEL [LANDY INTERNATIONAL ]1Legacy NDC, 2 package rows20100708_86256ff0-0a6d-44c0-82b0-4c086b116c20.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALCOHOLACTIVE INGREDIENT3K9958V90M1
ALCOHOLACTIVE MOIETY3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51706-20251706-202-01, 51706-202-02

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
NameUNIIKind
ALCOHOL3K9958V90MACTIB

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
024d5dcf-ac54-4317-bd9d-759d69634ac586256ff0-0a6d-44c0-82b0-4c086b116c202010-07-07WarningsExact identifier
spl id: 024d5dcf-ac54-4317-bd9d-759d69634ac5
spl set id: 86256ff0-0a6d-44c0-82b0-4c086b116c20

Reported adverse events (FAERS/openFDA)#

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