OTC Medication Information: UltraMax Invisible Solid – Unscented Antiperspirant Deodorant Unscented

ULTRAMAX INVISIBLE SOLID — UNSCENTED ANTIPERSPIRANT DEODORANT UNSCENTED- aluminum chlorohydrate stick
Church & Dwight Co., Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Aluminum Chlorohydrate 19%

Antiperspirant

Use reduces underarm perspiration

For external use only

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Apply a thin layer to underarms only

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

Questions or Comments?

Call 1-800-248-8820

M-F 9am-5pm ET

or visit www.ahultramax.com

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_front
(click image for full-size original)
ULTRAMAX INVISIBLE SOLID — UNSCENTED ANTIPERSPIRANT DEODORANT UNSCENTED
aluminum chlorohydrate stick
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10237-873
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
ALUMINUM CHLOROHYDRATE (ALUMINUM CHLOROHYDRATE) ALUMINUM CHLOROHYDRATE 0.19 g in 1 g
Inactive Ingredients
Ingredient Name Strength
ETHYLENE BRASSYLATE
C12-20 ALKYL BENZOATE
PETROLATUM
CYCLOMETHICONE 5
STEARYL ALCOHOL
PPG-14 BUTYL ETHER
TALC
HYDROGENATED CASTOR OIL
SODIUM BICARBONATE
STARCH, CORN
XANTHAN GUM
MALTODEXTRIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10237-873-26 73 g in 1 CANISTER None
2 NDC:10237-873-28 73 g in 1 CANISTER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part350 02/01/2021
Labeler — Church & Dwight Co., Inc. (001211952)
Establishment
Name Address ID/FEI Operations
Church & Dwight Co., Inc. 043690812 MANUFACTURE (10237-873)

Revised: 01/2023 Church & Dwight Co., Inc.

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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