FDA.reportPublic FDA data

Babaria Cotton Fresh Deodorant and Antiperspirant Liquid Roll-On

Manufacturer
BERIOSKA SL
Effective date
2025-12-20
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:27:31

Label at a glance#

ProductBabaria Cotton Fresh Deodorant and Antiperspirant Liquid Roll-On
Active ingredientALUMINUM CHLOROHYDRATE
Label structure6 sections

Indications and uses

Reduces underarm sweat 24 hour effective protection

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

  • Reduces underarm sweat
  • 24 hour effective protection

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken skin

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (aqua), steareth-2, glycerin, steareth-21, cotton (gossypium herbaceum) seed oil, octenidine HCL, tocopherol, Polysorbate 80, fragrance (parfum), sodium hydroxide, ethylhexylglycerin, phenoxyethanol, propylene glycol, dehydroacetic acid, benzoic acid, sorbic acid, decylene glycol, 1,2-hexanediol, citronellol, eugenol, hexyl cinnamal, linalool, alpha-isomethyl ionone.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138410412018524GTIN-13: 8410412018524
EAN-13: 8410412018524
GTIN storage (14 digits): 08410412018524		label.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
78283-002-01Babaria Cotton Fresh Deodorant and Antiperspirant Liquid Roll-On50 mL in 1 BOTTLEEMULSION504

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78283-00278283-002-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
STEARETH-2V56DFE46J5IACT
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
STEARETH-2153J3F32P58IACT
COTTONSEED OILH3E878020NIACT
OCTENIDINE HYDROCHLORIDEU84956NU4BIACT
TOCOPHEROLR0ZB2556P8IACT
POLYSORBATE 806OZP39ZG8HIACT
SODIUM HYDROXIDE55X04QC32IIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DEHYDROACETIC ACID2KAG279R6RIACT
BENZOIC ACID8SKN0B0MIMIACT
SORBIC ACIDX045WJ989BIACT
DECYLENE GLYCOLS57M60MI88IACT
1,2-HEXANEDIOLTR046Y3K1GIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
EUGENOL3T8H1794QWIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
LINALOOL, (+/-)-D81QY6I88EIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
Babaria Cotton Fresh Deodorant and Antiperspirant Liquid Roll-OnALUMINUM CHLOROHYDRATEBERIOSKA SLf1a9877a-fdb7-4e1c-8bc5-0b2b8b507f042025-12-20WarningsExact identifier
ndc (package): 78283-002-01
ndc (product): 78283-002
ndc11 (package): 78283000201
spl id: 4663aa4c-04cf-ab66-e063-6394a90a119b
spl set id: f1a9877a-fdb7-4e1c-8bc5-0b2b8b507f04

Reported adverse events (FAERS/openFDA)#

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