UltraMax Invisible Solid - Unscented

Manufacturer
Church & Dwight Co., Inc.
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 00:38:45

Label at a glance#

ProductUltraMax Invisible Solid - Unscented Antiperspirant Deodorant Unscented
Active ingredientALUMINUM CHLOROHYDRATE
Label structure12 sections

Dosage and administration

Apply a thin layer to underarms only

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate 19%

OTC - PURPOSE SECTION

Antiperspirant

INDICATIONS & USAGE SECTION

Usereduces underarm perspiration

WARNINGS SECTION

For external use only

OTC - DO NOT USE SECTION

Do not useon broken skin

OTC - STOP USE SECTION

Stop use ifrash or irritation occurs

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you havekidney disease

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 a thin layer to underarms only

INACTIVE INGREDIENT SECTION

PPG-14 Butyl Ether, Cyclopentasiloxane, Stearyl Alcohol, C12-15 Alkyl Benzoate, Talc, Hydrogenated Castor Oil, Petrolatum, Ethylene Brassylate, Sodium Bicarbonate (Baking Soda), Corn Starch Modified, Polysaccharides, Maltodextrin

OTC - QUESTIONS SECTION

Questions or Comments?

Call 1-800-248-8820

M-F 9am-5pm ET

or visit www.ahultramax.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

REDUCES

UNDERARM SWEAT

DUE TO STRESS

ARM AND HAMMER

THE STANDARD OF PURITY

ULTRA MAX

unscented

Antiperspirant Deodorant

SOLID

NET WT. 2.6 OZ. (73g)

UMLBF-19460-10_frontUMLBF-19460-10_front

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10237-873-26UltraMax Invisible Solid - UnscentedAntiperspirant Deodorant Unscented73 g in 1 CANISTERSTICK733
10237-873-28UltraMax Invisible Solid - UnscentedAntiperspirant Deodorant Unscented73 g in 1 CANISTERSTICK733

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10237-873ULTRAMAX INVISIBLE SOLID - UNSCENTED ANTIPERSPIRANT DEODORANT UNSCENTED (ALUMINUM CHLOROHYDRATE) STICK [CHURCH & DWIGHT CO., INC.]3Current NDC, Legacy NDC, 2 package rows20241123_b59340cb-4480-266b-e053-2995a90ac82d.zip

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
10237-87310237-873-26, 10237-873-28

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
UltraMax Invisible Solid - Unscented Antiperspirant Deodorant UnscentedALUMINUM CHLOROHYDRATEChurch & Dwight Co., Inc.b59340cb-4480-266b-e053-2995a90ac82d2024-11-20WarningsExact identifier
ndc (package): 10237-873-28
ndc (package): 10237-873-26
ndc (product): 10237-873
ndc11 (package): 10237087326
ndc11 (package): 10237087328
spl id: 2763645d-72fa-24ee-e063-6394a90af5de
spl set id: b59340cb-4480-266b-e053-2995a90ac82d

Reported adverse events (FAERS/openFDA)#

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