CLARISSE Antiperspirant Deodorant

Manufacturer: Delta Brands Inc
Effective date: 2019-04-17
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-02 00:25:40

Label at a glance#

ProductCLARISSE Antiperspirant Deodorant Daily Protection

Active ingredientALUMINUM CHLOROHYDRATE

Label structure11 sections

Dosage and administration

remove cap, turn dial to raise product, apply evenly to underarms only, replace cap after use.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm wetness and perspiration

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

on broken or irritated skin.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease

Stop use and ask a doctor

OTC - STOP USE SECTION

if irritation or rash develops

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, seek medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

remove cap, turn dial to raise product, apply evenly to underarms only, replace cap after use.

Inactive ingredients

INACTIVE INGREDIENT SECTION

mineral oil, stearic acid, stearyl alcohol, talc, zinc palmitate, cyclopentasiloxane, hydrogenated castor oil, fragrance, silica, PPG-14 butyl ether, PEG-8 distearate, butylated hydroxytoluene

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

package label

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

CLARISSE Antiperspirant Deodorant Daily Protection
Aluminum chlorohydrate
PPG-14 BUTYL ETHER
HYDROGENATED CASTOR OIL
STEARIC ACID
STEARYL ALCOHOL
TALC
SILICON DIOXIDE
ZINC PALMITATE
CYCLOMETHICONE 5
MINERAL OIL
PEG-8 DISTEARATE
BUTYLATED HYDROXYTOLUENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
20276-700	20276-700-57, 20276-700-64, 20276-700-71, 20276-700-51

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
PPG-14 BUTYL ETHER	R199TJT95T	IACT
HYDROGENATED CASTOR OIL	ZF94AP8MEY	IACT
STEARIC ACID	4ELV7Z65AP	IACT
STEARYL ALCOHOL	2KR89I4H1Y	IACT
TALC	7SEV7J4R1U	IACT
SILICON DIOXIDE	ETJ7Z6XBU4	IACT
ZINC PALMITATE	Q7407964JA	IACT
CYCLOMETHICONE 5	0THT5PCI0R	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB
MINERAL OIL	T5L8T28FGP	IACT
PEG-8 DISTEARATE	7JNC8VN07M	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
86bbb477-bc71-38cf-e053-2991aa0af4ae			3fb479a3-aea2-1b06-e054-00144ff8d46c	2019-04-17	Warnings	Exact identifier spl id: 86bbb477-bc71-38cf-e053-2991aa0af4ae spl set id: 3fb479a3-aea2-1b06-e054-00144ff8d46c

Reported adverse events (FAERS/openFDA)#

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