Old Spice Timber with Sandalwood Invisible

Product NDC
69423-441
11-digit product format
694230441
Labeler code
69423
Product ID
69423-441_a74684bb-a6ec-e058-e053-2a95a90a6b16
Type
HUMAN OTC DRUG
Nonproprietary name
Aluminum Zirconium Trichlorohydrex Gly
Dosage form
STICK
Route
TOPICAL
Labeler
The Procter & Gamble Manufacturing Company
Application
part350
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-11-20
Marketing end
0000-00-00
Substance
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Active strength
18 g/100g
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct69423-441DDiscontinued by firm2026-07-31
excluded packagepackage69423-44169423-441-01DDiscontinued by firm2026-07-31
excluded packagepackage69423-44169423-441-73DDiscontinued by firm2026-07-31
excluded packagepackage69423-44169423-441-96DDiscontinued by firm2026-07-31

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Antiperspirant Wipe for WomenALUMINUM CHLOROHYDRATEFlawlessWipes, LLCa94d0d85-2537-424f-87c8-6aeade0478002017-07-17WarningsExact identifier
Mitchum Advance ControlALUMINUM CHLOROHYDRATERevlon Consumer Products Corp40b9968a-9025-5ed9-e054-00144ff88e882016-12-07WarningsExact identifier

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

warnings

WARNINGS For external use only When using this product avoid contact with eyes. in case of eye contact, flush thoroughly with water. Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72 hours

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69423-441-01694230441012 CANISTER in 1 CELLO PACK (69423-441-01) > 73 g in 1 CANISTER2 canister2019-11-200000-00-00NoNoCurrent
69423-441-736942304417373 g in 1 CANISTER (69423-441-73) 73 g2019-11-200000-00-00NoNoCurrent
69423-441-966942304419696 g in 1 CANISTER (69423-441-96) 96 g2020-03-070000-00-00NoNoCurrent