Babaria Aloe Fresh Deodorant And Antiperspirant Liquid Roll-on Emulsion
FDA Label NDC 78283-001

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Berioska Sl for the product Babaria Aloe Fresh Deodorant And Antiperspirant Liquid Roll-on (NDC 78283-001). 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, do not use, stop use if, ask a doctor before use if, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Aluminum chlorohydrate 20%

Purpose

Antiperspirant

Uses

  • Reduces underarm sweat 
  • 24 hour effective protection

Warnings

For external use only

Do Not Use

on broken skin

Stop Use If

rash or irritation occurs

Ask A Doctor Before Use If

you have kidney disease

Keep Out Of Reach Of Children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply to underarms only

Inactive Ingredients

Water (aqua), steareth-2, steareth-21, glycerin, aloe barbadensis leaf extract, octenidine HCL, polysorbate 80, ethylhexylglycerin, fragrance (parfum), phenoxyethanol, sodium hydroxide, propylene glycol, dehydroacetic acid, benzoic acid, sorbic acid, citric acid, ascorbic acid, sodium sulfite, sodium benzoate, potassium sorbate.

Package Labeling:

Label01 (Label01)

Label01 (Label01)

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