Babaria Skin Natural Fresh Deodorant and Antiperspirant Liquid Roll-On
Aluminum Chlorohydrate · Emulsion · Topical
Active ingredient
Active ingredient Aluminum chlorohydrate 20% Purpose Antiperspirant
Purpose
Purpose Antiperspirant
Uses
Uses
• Reduces underarm sweat
• 24 hour effective protection
Warnings
Warnings For external use only Do not use on broken skin Stop use if 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.
Do not use
Do not use on broken skin
Ask a doctor before use
Ask a doctor before use if you have kidney disease
Stop use and ask a doctor
Stop use if if rash or irritation occurs
Keep out of reach of children
Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away.
Directions
Directions Apply to underarms only
Inactive ingredients
Inactive ingredients Water (aqua), steareth-2, glycerin, steareth-21, octenidine HCL, polysorbate 80, ethylhexylglycerin, propylene glycol, fragrance (parfum), phenoxyethanol, sodium hydroxide, dehydroacetic acid, benzoic acid, sorbic acid, benzyl alcohol, citronellol, limonene, linalool, alpha-isomethyl ionone.
Label text from the FDA structured product label by BERIOSKA SL (revised Dec 20, 2025). Long sections are shortened; the complete label is on DailyMed.
Active ingredients
- Aluminum Chlorohydrate in 1 product
Babaria Skin Natural Fresh Deodorant and Antiperspirant Liquid Roll-On NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 78283-007 | Aluminum Chlorohydrate 200 mg/mL Emulsion | BERIOSKA SL | OTC MONOGRAPH DRUG |
Frequently asked questions
What is Babaria Skin Natural Fresh Deodorant and Antiperspirant Liquid Roll-On used for?
Uses • Reduces underarm sweat • 24 hour effective protection
Who makes Babaria Skin Natural Fresh Deodorant and Antiperspirant Liquid Roll-On?
Babaria Skin Natural Fresh Deodorant and Antiperspirant Liquid Roll-On is listed by 1 labeler in the FDA NDC directory, including BERIOSKA SL.