Lady Speed Stick

Manufacturer
Colgate-Palmolive Company
Effective date
2019-12-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:18:43

Label at a glance#

ProductLady Speed Stick 24/7 Fresh Fusion
Active ingredientALUMINUM CHLOROHYDRATE
Label structure10 sections

Dosage and administration

Apply to underarms only

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 12%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

Reduces underarm wetness

Warnings

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not use on broken skin

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have kidney disease

OTC - STOP USE SECTION

Stop use if skin 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

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, hydrogenated soybean oil, steareth-2, PPG-15 stearyl ether, steareth-20, fragrance, caprylyl glycol, tetrasodium EDTA, BHT.

Questions or comments?

OTC - QUESTIONS SECTION

Call toll-free 1-800-228-7408

SPL UNCLASSIFIED SECTION

Dist. by:
COLGATE-PALMOLIVE COMPANY
New York, NY 10022

PRINCIPAL DISPLAY PANEL - 50mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Non-Stop
Protection

fresh
fusion®

lady
Speed
Stick
®

24/7
WETNESS & ODOR PROTECTION

antiperspirant/deodorant
1.7 FL OZ (50mL)
ROLL-ON

481478

PRINCIPAL DISPLAY PANEL - 50mL Bottle Label
PRINCIPAL DISPLAY PANEL - 50mL Bottle Label

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
35000-97635000-976-77

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Source Document#

Source XML · Source PDF

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
a3ffc08b-dd94-4b11-8478-73500413df1f85e01631-c93b-49ae-a09b-ce4004b0288d2019-12-20WarningsExact identifier
spl id: a3ffc08b-dd94-4b11-8478-73500413df1f
spl set id: 85e01631-c93b-49ae-a09b-ce4004b0288d

Reported adverse events (FAERS/openFDA)#

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