BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING

Manufacturer
Robanda International, Inc.
Effective date
2025-01-08
Label type
HUMAN OTC DRUG LABEL
Version
6
Source
full-release
Hydrated at
2026-06-01 00:51:39

Label at a glance#

ProductBODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING
Active ingredientALCOHOL
Label structure9 sections

Indications and uses

Works instantly to effectively eliminate germs and bacteria from cosmetic products, tester displays, makeup kits, workstations or hands

Dosage and administration

Hold spray 6” away from products, hands and surfaces, gently spray once or twice from one side to the other, in a swiping motion.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

ETHANOL (Alcohol Denat.) 60.00%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

uses

INDICATIONS & USAGE SECTION

Works instantly to effectively eliminate germs and bacteria from cosmetic products, tester displays, makeup kits, workstations or hands

Warnings

WARNINGS SECTION

Flammable. Keep away from fire or flame.
Do not use in or near the eyes, in case of contact, rinse thoroughly with water.
For external use only. Stop use and ask a doctor if irritation or rash appears and lasts. Avoid contact with broken skin.

If swallowed, seek medical help immediately.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

Directions

DOSAGE & ADMINISTRATION SECTION

  • Hold spray 6” away from products, hands and surfaces, gently spray once or twice from one side to the other, in a swiping motion.

OTHER INFORMATION

OTHER SAFETY INFORMATION

  • Store between 15-30C (56-86F)
  • Avoid freezing and excessive heat about 40C (104F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), Citrullus lanatus (Watermelon) Fruit Extract, Chenopodium quinoa Extract, Urea, Sucrose, Glycerin, Sodium Lactate, Sodium
PCA, Phenoxyethanol, Ethylhexylglycerin, Caprylyl Glycol, Hexylene Glycol, Fragrance

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_Bodyographypro_Antibacterial Cosmetic Sanitizer_4oz01b LBL_Bodyographypro_Antibacterial Cosmetic Sanitizer_4oz

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1367692ethanol 60 % Topical SprayPSN6
1367692ethanol 0.6 ML/ML Topical SpraySCD6
1367692ethanol 60 % Topical SpraySY6

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
444b3e50-f226-46ef-bfca-2e7035d140cdProduct name120190611
597b1cfd-7b31-5048-62be-ca5cd740da2fProduct name120140508
ec2149b3-5c6d-5344-f757-c86411073075Product name120140508

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
53950-6010-1BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING118 mL in 1 BOTTLESPRAY1186

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
53950-6010BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZING (ETHYL ALCOHOL) SPRAY [ROBANDA INTERNATIONAL, INC.]6Current NDC, Legacy NDC, 1 package rows20250110_ebec43d4-4676-40f9-b989-5381f4a737c8.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
53950-601053950-6010-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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
BODYOGRAPHYPRO ANTI-BACTERIAL SANITIZINGETHYL ALCOHOLRobanda International, Inc.ebec43d4-4676-40f9-b989-5381f4a737c82025-01-08WarningsExact identifier
ndc (package): 53950-6010-1
ndc (product): 53950-6010
ndc11 (package): 53950601001
spl id: 2b370bb8-bb61-f263-e063-6394a90a1ccd
spl set id: ebec43d4-4676-40f9-b989-5381f4a737c8

Reported adverse events (FAERS/openFDA)#

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