FDA.reportPublic FDA data

Old Spice Bow to the Kingram

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-08-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-08-08 02:02:25

Label at a glance#

ProductOld Spice Bow to the Kingram
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 19% (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, C12-15 alkyl benzoate, hydrogenated castor oil, fragrance, petrolatum, cyclodextrin, ozokerite, C20-40 alketh-10, corn starch/maltodextrin crosspolymer, kaolin, behenyl alcohol, bisabolol, panthenyl triacetate, tocopheryl acetate, sodium hyaluronate, zingiber officinale (ginger) root extract

Questions?

OTC - QUESTIONS SECTION

1-800-677-7582

SPL UNCLASSIFIED SECTION

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

PRINCIPAL DISPLAY PANEL - 73 g Cylinder Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Old Spice Bow to the Kingram

ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY

ANTIPERSPIRANT/DEODORANT

NET WT. 2.6 OZ (73 g)

SCENT OF COGNAC and CARRIES

OSOS

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130012044072240GTIN-13: 0012044072240
EAN-13: 0012044072240
GTIN-12: 012044072240
UPC-A: 012044072240
GTIN storage (14 digits): 00012044072240		OS.jpg
Data codeData Matrix21530906OS.jpg

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-29284126-292-73

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLY8O386558JEACTIB
C12-15 ALKYL BENZOATEA9EJ3J61HQIACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
CERESINQ1LS2UJO3AIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
C20-40 PARETH-10TE3MZI4V3FIACT
BEHENYL ALCOHOL9G1OE216XYIACT
PETROLATUM4T6H12BN9UIACT
MINERAL OILT5L8T28FGPIACT
CYCLODEXTRINS7E6SK9QDT8IACT
KAOLIN24H4NWX5COIACT
BISABOLOL24WE03BX2TIACT
PANTHENYL TRIACETATE1206E8961BIACT
ALPHA-TOCOPHEROL ACETATE9E8X80D2L0IACT
SODIUM HYALURONATEYSE9PPT4THIACT
GINGERC5529G5JPQIACT

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
Old Spice Bow to the KingramALUMINUM ZIRCONIUM TETRACHLOROHYDREX GLYThe Procter & Gamble Manufacturing Company5863e3bd-776b-56ae-e063-6294a90a19ef2026-08-06WarningsExact identifier
ndc (package): 84126-292-73
ndc (product): 84126-292
ndc11 (package): 84126029273
spl id: 5863e396-b023-57a6-e063-6294a90a1961
spl set id: 5863e3bd-776b-56ae-e063-6294a90a19ef

Reported adverse events (FAERS/openFDA)#

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