Bodyographypro Anti-bacterial Sanitizing Spray
FDA Label NDC 53950-6010

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Robanda International, Inc. for the product Bodyographypro Anti-bacterial Sanitizing (NDC 53950-6010). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHANOL (Alcohol Denat.) 60.00%

Purpose

Antimicrobial

Uses

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

Warnings

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

KEEP OUT OF REACH OF CHILDREN

Directions

  • 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

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

Inactive Ingredients

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

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