Babaria Oat Fresh Deodorant And Antiperspirant Liquid Roll-on Emulsion
FDA Label NDC 78283-005

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 Oat Fresh Deodorant And Antiperspirant Liquid Roll-on (NDC 78283-005). 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 drug facts, active ingredient, purpose, uses, warnings, do not use, stop use if, ask a doctor before use if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

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 Posion Control Center right away.

Directions

Apply to underarms only

Inactive Ingredients

Water (aqua), steareth-2, glycerin, steareth-21, oat (avena sativa) kernel extract, octenidine HCL, ethylhexylglycerin, propylene glycol, Polysorbate 80, fragrance (parfum), phenoxyethanol, sodium hydroxide, dehydroacetic acid, benzoic acid, sorbic acid, potassium sorbate, sodium benzoate, D&C Yellow No.10 (CI 47005), FD&C Yellow No.5 (CI 19140), FD&C Red No.40 (CI 16035), benzyl alcohol, citronellol, coumarin, eugenol, hexyl cinnamal, linalool, alpha-isomethyl ionone.

Package Labeling:

Bottle3 (Bottle3)

Bottle3 (Bottle3)

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