FDA.reportPublic FDA data

Carpe Antiperspirant Underarm Bergamot and Oud Scent

Manufacturer
Cosco International, Inc.
Effective date
2025-03-31
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:58:19

Label at a glance#

ProductCarpe Antiperspirant Underarm Bergamot and Oud Scent
Active ingredientAluminum Sesquichlorohydrate
Label structure9 sections

Dosage and administration

Apply to underarms only Rotate knob to dispense product and rub in vigorously  For best results, apply every night before bed and again in the morning

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient                                                      Purpose
Aluminum Sesquicholorhydrate 15% .......................Anti-perspirant

OTC - PURPOSE SECTION

Anti-perspirant

Use

INDICATIONS & USAGE SECTION

  • Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • on broken or irritated skin

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • rash or irritation occurs

Ask 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 Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only
  • Rotate knob to dispense product and rub in vigorously 
  • For best results, apply every night before bed and again in the morning

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water (Aqua), Glyceryl Stearate SE, Silica, Silica Silylate, Glycerin, Dimethicone, Ethylhexyl Palmitate, Cetyl Alcohol, Cetearyl Alcohol, Fragrance, Isopropyl Myristate, Phenoxyethanol, Hydroxypropyl Methylcellulose, Ethylhexylglycerin, Sodium Hydroxide 

Questions?

OTC - QUESTIONS SECTION

Call 888-621-0135

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50ml label50ml label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52261-4733-1Carpe Antiperspirant Underarm Bergamot and Oud Scent0.050 kg in 1 TUBELotion0.0505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52261-4733CARPE ANTIPERSPIRANT UNDERARM BERGAMOT AND OUD SCENT (ALUMINUM SESQUICHLOROHYDRATE) LOTION [COSCO INTERNATIONAL, INC.]5Current NDC, 1 package rows20250402_9e1ce7c6-b951-4a57-b7f0-9f0a591e4778.zip

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52261-473352261-4733-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum SesquichlorohydrateUCN889409VACTIB
water059QF0KO0RIACT
CETOSTEARYL ALCOHOL2DMT128M1SIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HEXAMETHYLDISILAZANEH36C68P1BHIACT
GLYCERINPDC6A3C0OXIACT
ETHYLHEXYL PALMITATE2865993309IACT
dimethicone 3502Y53S6ATLUIACT
GLYCERYL STEARATE SEFCZ5MH785IIACT
phenoxyethanolHIE492ZZ3TIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
SODIUM HYDROXIDE55X04QC32IIACT
HYPROMELLOSE 2208 (100000 MPA.S)VM7F0B23ZIIACT
ethylhexylglycerin147D247K3PIACT
CETYL ALCOHOL936JST6JCNIACT

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
Carpe Antiperspirant Underarm Bergamot and Oud ScentALUMINUM SESQUICHLOROHYDRATECosco International, Inc.9e1ce7c6-b951-4a57-b7f0-9f0a591e47782025-03-31WarningsExact identifier
ndc (package): 52261-4733-1
ndc (product): 52261-4733
ndc11 (package): 52261473301
spl id: 387be773-8c53-4329-8638-0edd62f2feaa
spl set id: 9e1ce7c6-b951-4a57-b7f0-9f0a591e4778

Reported adverse events (FAERS/openFDA)#

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