LUMISTE NOIR BLACK

Manufacturer
COCO COSMETICS INC
Effective date
2025-11-09
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
monthly-update
Hydrated at
2026-06-03 17:45:08

Label at a glance#

ProductLUMISTE NOIR BLACK
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Dosage and administration

• Apply to underarms only • Use on clean, dry skin • Let dry before dressing

Storage and handling

• Protect from excessive heat and direct sunlight • Store at 20-250C (68-770F) • See bottom of packaging for lot number and expiration date

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 12.0%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

48-hour protection

Warnings

WARNINGS SECTION

For external use only.

Do not use on damaged skin.

Stop use if rash or irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Apply to underarms only

• Use on clean, dry skin

• Let dry before dressing

Other information

STORAGE AND HANDLING SECTION

• Protect from excessive heat and direct sunlight

• Store at 20-250C (68-770F)

• See bottom of packaging for lot number and expiration date

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aqua, Dicaprylyl Carbonate,

Steareth-2, Parfum, Steareth-21 , Dimethicone, 2-Methyl

5-Cyclohexylpentanol

Package Label - Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Products#

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DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87093-11587093-115-75

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 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
527d88e4-46d0-50bf-e063-6394a90a0d9e432f4a21-e327-e178-e063-6394a90ad2312026-05-23WarningsExact identifier
spl set id: 432f4a21-e327-e178-e063-6394a90ad231

Reported adverse events (FAERS/openFDA)#

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