Carpe Antiperspirant Underarm Fresh Powder Scent

Manufacturer
Cosco International, Inc.
Effective date
2025-02-04
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:54:24

Label at a glance#

ProductCarpe Antiperspirant Underarm Fresh Powder 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, Cetostearyl Alcohol, Silica, Silica Silylate, Glycerin, Dimethicone, Ethylhexyl Palmitate, Glyceryl Stearate, Isopropyl Myristate, Fragrance, Sodium Hydroxide, Phenoxyethanol, Hydroxypropyl Methylcellulose, Ethylhexylglycerin 

Questions?

OTC - QUESTIONS SECTION

Call 888-621-0135

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

50ml inner package label50ml inner package label50ml outer package label50ml outer package label

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
52261-4719-02025-02-04C16284748780-12cef2736-a0e9-d83d-e063-dadaa90ab31fDrug Facts
52261-4719-02025-01-30C16284748780-12cef2736-a0e9-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52261-4719-0Carpe Antiperspirant Underarm Fresh Powder Scent1 in 1 CARTONLotion15
52261-4719-1Carpe Antiperspirant Underarm Fresh Powder Scent0.050 kg in 1 TUBELotion0.0505

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52261-4719CARPE ANTIPERSPIRANT UNDERARM FRESH POWDER SCENT (ALUMINUM SESQUICHLOROHYDRATE) LOTION [COSCO INTERNATIONAL, INC.]5Current NDC, Legacy NDC, 2 package rows20250206_b8cac022-3da2-495e-ad6a-e067bd859ca2.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52261-471952261-4719-1, 52261-4719-0

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

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 Fresh Powder ScentALUMINUM SESQUICHLOROHYDRATECosco International, Inc.b8cac022-3da2-495e-ad6a-e067bd859ca22025-02-04WarningsExact identifier
ndc (package): 52261-4719-0
ndc (package): 52261-4719-1
ndc (product): 52261-4719
ndc11 (package): 52261471901
ndc11 (package): 52261471900
spl id: 56196e62-d4b6-4b0b-af8e-e7a00449ad4c
spl set id: b8cac022-3da2-495e-ad6a-e067bd859ca2

Reported adverse events (FAERS/openFDA)#

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