FDA.reportPublic FDA data

Carpe Antiperspirant Hand Rose Water Scent

Manufacturer
Cosco International, Inc.
Effective date
2023-12-27
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:05:50

Label at a glance#

ProductCarpe Antiperspirant Hand Rose Water Scent
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure9 sections

Dosage and administration

Wash and dry hands throughly before application Apply a small, pea-sized amount of Carpe to palms Rub palms together vigorously for 15 seconds 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 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

  • Wash and dry hands throughly before application
  • Apply a small, pea-sized amount of Carpe to palms
  • Rub palms together vigorously for 15 seconds
  • 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

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

Questions?

OTC - QUESTIONS SECTION

Call 888-621-0135

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

40ml label
40ml label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52261-4730-12025-01-30C16284748780-12cef2736-6d54-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52261-4730-1Carpe Antiperspirant Hand Rose Water Scent0.04738 kg in 1 TUBELotion0.047388

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52261-4730CARPE ANTIPERSPIRANT HAND ROSE WATER SCENT (ALUMINUM SESQUICHLOROHYDRATE) LOTION [COSCO INTERNATIONAL, INC.]81 package rows20231228_cbf0d17d-d489-4a59-bcbf-022ea960ec90.zip

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
52261-473052261-4730-1

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
8062d4d6-9621-4524-b61e-dbb45bc3b68fcbf0d17d-d489-4a59-bcbf-022ea960ec902023-12-27WarningsExact identifier
spl id: 8062d4d6-9621-4524-b61e-dbb45bc3b68f
spl set id: cbf0d17d-d489-4a59-bcbf-022ea960ec90

Reported adverse events (FAERS/openFDA)#

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