FDA.reportPublic FDA data

Carpe Antiperspirant Underarm Coastal Orange Scent

Manufacturer
Cosco International, Inc.
Effective date
2023-01-24
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:39:25

Label at a glance#

ProductCarpe Antiperspirant Underarm Coastal Orange Scent
Active ingredientAluminum Sesquichlorohydrate
Label structure10 sections

Dosage and administration

Apply to underarms only Squeeze product from tube and rub in vigorously  For best results, apply every night before bed and an additional two times per day for at least four weeks

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
  • Squeeze product from tube and rub in vigorously 
  • For best results, apply every night before bed and an additional two times per day for at least four weeks

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Isopropyl Alcohol, Silica, Silica Silylate, Talc, Polysorbate-20, Dimethicone, C12-15 Alkyl Benzoate, Fragrance, Phenoxyethanol, Isopropyl Myristate, Glycerin, Hydroxypropyl Methylcellulose, Ethylhexylglycerin, Citric Acid, Sodium Hydroxide 

Questions?

OTC - QUESTIONS SECTION

Call 888-621-0135

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

15ml label15ml label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

60ml label60ml label

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52261-470652261-4706-1, 52261-4706-3

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
NameUNIIKind
Aluminum SesquichlorohydrateUCN889409VACTIB
water059QF0KO0RIACT
isopropyl alcoholND2M416302IACT
SILICON DIOXIDEETJ7Z6XBU4IACT
HEXAMETHYLDISILAZANEH36C68P1BHIACT
talc7SEV7J4R1UIACT
polysorbate 207T1F30V5YHIACT
dimethicone 3502Y53S6ATLUIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
phenoxyethanolHIE492ZZ3TIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
glycerinPDC6A3C0OXIACT
HYPROMELLOSE 2208 (100000 MPA.S)VM7F0B23ZIIACT
sodium hydroxide55X04QC32IIACT
citric acid monohydrate2968PHW8QPIACT
ethylhexylglycerin147D247K3PIACT

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
655cea6d-739c-452e-b4ae-ff314f1d9ea5cf49d5cd-c7f2-4b33-abcd-830ee092239a2024-01-10WarningsExact identifier
spl set id: cf49d5cd-c7f2-4b33-abcd-830ee092239a

Reported adverse events (FAERS/openFDA)#

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