FDA.reportPublic FDA data

Old Spice Midnight Run

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2020-02-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 23:42:00

Label at a glance#

ProductOld Spice Midnight Run
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX 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 trichlorohydrex Gly 18% (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, dimethicone, talc, petrolatum, fragrance, hydrogenated castor oil, PPG-14 butyl ether, cyclodextrin, behenyl alcohol

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 96 g Cylinder Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Old Spice

Midnight Run

ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
ANTIPERSPIRANT/DEODORANT

NET WT. 3.4 OZ (96 g)

OSOS

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69423-269-962020-02-03C16284748780-19d75b9cf-faaf-f424-e053-dadaa90a57ceOld Spice Midnight Run Invisible Solid
69423-269-962020-01-31C16284748780-19d75b9cf-faaf-f424-e053-dadaa90a57ceOld Spice Midnight Run Invisible Solid

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69423-26969423-269-96

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
DOCOSANOL9G1OE216XYIACT
PETROLATUM4T6H12BN9UIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CYCLOMETHICONE 50THT5PCI0RIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
DIMETHICONE92RU3N3Y1OIACT
MINERAL OILT5L8T28FGPIACT
TALC7SEV7J4R1UIACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB
PPG-14 BUTYL ETHERR199TJT95TIACT
BETADEXJV039JZZ3AIACT

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
9db2cc3f-05e9-077c-e053-2a95a90a78136f27638c-ed12-bf6b-e053-2991aa0a57cb2020-02-03WarningsExact identifier
spl id: 9db2cc3f-05e9-077c-e053-2a95a90a7813
spl set id: 6f27638c-ed12-bf6b-e053-2991aa0a57cb

Reported adverse events (FAERS/openFDA)#

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