FDA.reportPublic FDA data

Babaria Invisible 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 01:27:16

Label at a glance#

ProductBabaria Invisible 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 mediacal 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, niacinamide, ethylhexylglycerin, octenidine HCL, dimethicone, fragrance (parfum), sodium hydroxide, phenoxyethanol, propylene glycol, dehydroacetic acid, benzoic acid, sorbic acid, citronellol, limonene, 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-138410412018548GTIN-13: 8410412018548
EAN-13: 8410412018548
GTIN storage (14 digits): 08410412018548		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
78283-004-01Babaria Invisible 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 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78283-00478283-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
GLYCERINPDC6A3C0OXIACT
STEARETH-2153J3F32P58IACT
NIACINAMIDE25X51I8RD4IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
OCTENIDINE HYDROCHLORIDEU84956NU4BIACT
DIMETHICONE92RU3N3Y1OIACT
SODIUM HYDROXIDE55X04QC32IIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
DEHYDROACETIC ACID2KAG279R6RIACT
BENZOIC ACID8SKN0B0MIMIACT
SORBIC ACIDX045WJ989BIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
LIMONENE, (+)-GFD7C86Q1WIACT
LINALOOL, (+/-)-D81QY6I88EIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
32025-10-02legacy-cache2026-10-21 23:52:38

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 Invisible Deodorant and Antiperspirant Liquid Roll-OnALUMINUM CHLOROHYDRATEBERIOSKA SL7e6dffe7-4554-4b55-91b5-9d45bbd979132025-12-20WarningsExact identifier
ndc (package): 78283-004-01
ndc (product): 78283-004
ndc11 (package): 78283000401
spl id: 4663c74e-8c63-5d69-e063-6294a90a26db
spl set id: 7e6dffe7-4554-4b55-91b5-9d45bbd97913

Reported adverse events (FAERS/openFDA)#

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