Old Spice Timber with Sandalwood

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2020-02-04
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 23:41:53

Label at a glance#

ProductOld Spice Timber with Sandalwood
Active ingredientALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
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 zirconium tetrachlorohydrex Gly 15% (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

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, stearyl alcohol, mineral oil, PPG-14 butyl ether, hydrogenated castor oil, petrolatum, fragrance, talc, cyclodextrin, ozokerite,C20-40 pareth-10, fusanus spicatus wood (sandalwood) oil, behenyl alcohol.

Questions?

OTC - QUESTIONS SECTION

1-800-677-7582

SPL UNCLASSIFIED SECTION

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202.

PRINCIPAL DISPLAY PANEL - 73 g Cylinder

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Old Spice

TIMBER

with SANDALWOOD

ANTI-PERSPIRANT

& DEODORANT

ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY
ANTI-PERSPIRANT/DEODORANT

NET WT. 2.6 OZ (73 g)

OSOS

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-28969423-289-48, 69423-289-73, 69423-289-96, 69423-289-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
9dc1fe1d-ea0f-bf5c-e053-2a95a90acc077a1ae82e-31d4-198d-e053-2a91aa0aa9ad2020-02-04WarningsExact identifier
spl id: 9dc1fe1d-ea0f-bf5c-e053-2a95a90acc07
spl set id: 7a1ae82e-31d4-198d-e053-2a91aa0aa9ad

Reported adverse events (FAERS/openFDA)#

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