Old Spice On-The-Go No Melt

Manufacturer: The Procter & Gamble Manufacturing Company
Effective date: 2021-01-26
Label type: HUMAN OTC DRUG LABEL
Version: 2
Source: legacy-cache
Hydrated at: 2026-08-01 22:54:37

Label at a glance#

ProductOld Spice On-The-Go No Melt Clean Scent

Active ingredientALUMINUM CHLOROHYDRATE

Label structure10 sections

Dosage and administration

apply to underarms only Distribute product evenly over the armpit

Contacts and useful links#

PhoneLabel contact1-800-677-7582

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 14% (anhydrous)

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 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
Distribute product evenly over the armpit

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, PPG-15 stearyl ether, steareth-2, fragrance, steareth-20, disodium EDTA, BHT

Questions?

OTC - QUESTIONS SECTION

1-800-677-7582

SPL UNCLASSIFIED SECTION

Made in Canada

Distr. by

PROCTER & GAMBLE,

CINCINNATI, OH

45202.

PRINCIPAL DISPLAY PANEL - 53 mL Canister Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Old Spice _®

ON-THE-GO

NO MELT

CLEAN SCENT

Aluminum chlorohydrate
ANTI-PERSPIRANT

1.8 FL OZ (53 mL)

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

Old Spice On-The-Go No Melt Clean Scent
ALUMINUM CHLOROHYDRATE
WATER
PPG-15 STEARYL ETHER
STEARETH-2
STEARETH-20
EDETATE DISODIUM
BUTYLATED HYDROXYTOLUENE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
69423-420	69423-420-53

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
PPG-15 STEARYL ETHER	1II18XLS1L	IACT
STEARETH-2	V56DFE46J5	IACT
STEARETH-20	L0Q8IK9E08	IACT
EDETATE DISODIUM	7FLD91C86K	IACT
BUTYLATED HYDROXYTOLUENE	1P9D0Z171K	IACT
ALUMINUM CHLOROHYDRATE	HPN8MZW13M	ACTIB

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
b9d5aa82-4cc7-5442-e053-2995a90a4780			968c8e64-945e-430f-e053-2a95a90af004	2021-01-26	Warnings	Exact identifier spl id: b9d5aa82-4cc7-5442-e053-2995a90a4780 spl set id: 968c8e64-945e-430f-e053-2a95a90af004

Reported adverse events (FAERS/openFDA)#

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