FDA.reportPublic FDA data

Lactovit Deodorant Antiperspirant Lactourea

Manufacturer
AC MARCA PERSONAL CARE, S.L. | Laboratorio Genove, S.A.
Effective date
2020-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:23:34

Label at a glance#

ProductLactovit Deodorant Antiperspirant Lactourea
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

Aluminum chlorohydrate 10%

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.

In 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

OTC - ASK DOCTOR SECTION

before use if you have kidney disease.

Stop use and ask a doctor if

OTC - STOP USE SECTION

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:

SPL UNCLASSIFIED SECTION

Store at room temperature.

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, steareth-2, PPG-15 stearyl ether, steareth-21,fragrance, butylene glycol, xanthan gum, hydrolyzed milk protein, calcium lactate, sodium lactate, tocopheryl acetate, tocopherol, niacinamide, allantoin, hydroxyethyl urea, propanediol, bisabolol, farnesol, lecithin, glycine, polyglyceryl-3 caprylate, cyclopentasiloxane, helianthus annus (sunflower) seed oil, disodium EDTA, VP/eicosene copolymer, phenoxyethanol, alpha isomethyl ionone,  citral, citronellol, coumarin, limonene, geraniol, hexyl cinnamal, butylphenyl methylpropional, linalool,hydroxycitronellal.

Questions or comments:

OTC - QUESTIONS SECTION

+ 1-787-780-4043

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Label6Label6

Products#

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

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
42283-04542283-045-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 32 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
STEARETH-2V56DFE46J5IACT
PPG-15 STEARYL ETHER1II18XLS1LIACT
STEARETH-2153J3F32P58IACT
BUTYLENE GLYCOL3XUS85K0RAIACT
XANTHAN GUMTTV12P4NEEIACT
CALCIUM LACTATE2URQ2N32W3IACT
SODIUM LACTATETU7HW0W0QTIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
TOCOPHEROLR0ZB2556P8IACT
NIACINAMIDE25X51I8RD4IACT
ALLANTOIN344S277G0ZIACT
HYDROXYETHYL UREAMBQ7DDQ7ARIACT
PROPANEDIOL5965N8W85TIACT
LEVOMENOL24WE03BX2TIACT
FARNESOLEB41QIU6JLIACT
GLYCINETE7660XO1CIACT
CYCLOMETHICONE 50THT5PCI0RIACT
SUNFLOWER OIL3W1JG795YIIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ISOMETHYL-.ALPHA.-IONONE9XP4LC555BIACT
CITRALT7EU0O9VPPIACT
.BETA.-CITRONELLOL, (R)-P01OUT964KIACT
COUMARINA4VZ22K1WTIACT
LIMONENE, (+)-GFD7C86Q1WIACT
GERANIOLL837108USYIACT
.ALPHA.-HEXYLCINNAMALDEHYDE7X6O37OK2IIACT
BUTYLPHENYL METHYLPROPIONALT7540GJV69IACT
LINALOOL, (+/-)-D81QY6I88EIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
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
0797f914-1106-0eec-e063-6394a90a91a7350986d4-bf7f-4e66-a123-4f586bce6ff92023-10-13WarningsExact identifier
spl set id: 350986d4-bf7f-4e66-a123-4f586bce6ff9

Reported adverse events (FAERS/openFDA)#

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