FDA.reportPublic FDA data

LACTOVIT MEN DEODORANT AND ANTIPERSPIRANT

Manufacturer
AC Marca Personal Care
Effective date
2021-12-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 22:24:51

Label at a glance#

ProductLACTOVIT MEN DEODORANT AND ANTIPERSPIRANT
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Indications and uses

Reduces underarm wetness.

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminium chlorohydrate 12.0%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm wetness.

Warning

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken skin.

SPL UNCLASSIFIED SECTION

In case of accidentalIn case of accidental ingestion seek Professional Assistance or contact a Poison Control Center immediately.
Keep away from face and mouth.

Ask a Doctor or pharmacists before use if you have kidney disease.

OTC - ASK DOCTOR SECTION

Stop use and ask a doctor

OTC - STOP USE SECTION

if rash or irritation occurs.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to underarms only.

Other information:

OTHER SAFETY INFORMATION

Store at room temparature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, steareth-2, PPG-15 stearyl ether, steareth-21, butylene glycol, fragrance, hydrolyzed milk protein, calcium lactate, tocopheryl acetate, allantoin, triclosan, cyclopentasiloxane, disodium EDTA, VP/eicosene copolymer, phenoxyethanol, alpha isomethyl ionone,limonene.

Questions or comments:

OTC - QUESTIONS SECTION

+ 1-787-780-4043

Package Labeling

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LACTOVIT MEN DEODORANT AND ANTIPERSPIRANT.LACTOVIT MEN DEODORANT AND ANTIPERSPIRANT.

Products#

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

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42283-02742283-027-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2153J3F32P58IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
CALCIUM LACTATE2URQ2N32W3IACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALLANTOIN344S277G0ZIACT
TRICLOSAN4NM5039Y5XIACT
CYCLOMETHICONE 50THT5PCI0RIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
LIMONENE, (+)-GFD7C86Q1WIACT
ALUMINUM CHLOROHYDRATEHPN8MZW13MACTIB

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
d240f9da-6ae9-fb07-e053-2995a90aa93663f2bf2c-d1d1-4941-e053-2a91aa0a26b72021-12-03WarningsExact identifier
spl id: d240f9da-6ae9-fb07-e053-2995a90aa936
spl set id: 63f2bf2c-d1d1-4941-e053-2a91aa0a26b7

Reported adverse events (FAERS/openFDA)#

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