Lacura Extreme Blast
FDA Label NDC 10889-110

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Vvf Kansas Services Llc for the product Lacura Extreme Blast (NDC 10889-110). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, directions, storage and handling, inactive ingredients, other, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Active Ingredient

Aluminum Zirconium Trichlorohydrex Gly 20%

Purpose

Anti-perspirant

Uses

Reduces underarm wetness.

Warnings

For external use only. 

Do not use on broken skin. 

Ask a doctor before you use if you have kidney disease.

Stop use if rash or irritation occurs.

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center immediately.




Directions

Apply evenly to underarms only.

Storage And Handling

Do not store over 115 degrees F

Inactive Ingredients

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, Hydrogenated Castor  Oil, Zinc Ricinoleate, Fragrance, Talc, PEG-8 Distearate.

Other

Distributed By:

ALDI INC.
BATAVIA, IL
60510
(MI01.89CT)

100% Satisfaction Guaranteed
www.ALDI.us

Otc - Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center immediately.

Package Label.Principal Display Panel



Lacuraextremeblast Label (Lacuraextremeblast)

Lacuraextremeblast Label (Lacuraextremeblast)


Lacura

For Men
Extreme Blast
Antiperspirant +Deodorant
Lasting Protection
Invisible Stick

NET WT. 2.7OZ (76g)

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