FDA.reportPublic FDA data

HYDROFLUOROCARBON 152A - Suave Brands Co, LLC | EUROPEAN PERFUME WORKS CO. LLC

Manufacturer
Suave Brands Co, LLC | EUROPEAN PERFUME WORKS CO. LLC
Effective date
2026-03-26
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:51:39

Label at a glance#

ProductSuave Dry Antiperspirant Deodorant Powder and Petals
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients Aluminum Chlorohydrate

INACTIVE INGREDIENT SECTION

Inactive Ingredients Hydrofluorocarbon 152A, Butane, Cyclopentasiloxane, Propane, Isobutane, PPG-14 Butyl Ether, Fragrance (Parfum), Disteardimonium Hectorite, Propylene Carbonate, BHT, Cinnamyl Alcohol

OTC - PURPOSE SECTION

Purpose antiperspirant 

INDICATIONS & USAGE SECTION

Use reduces underarm wetness

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Warnings

  • FLAMMABLE, DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH.
  • Keep away from face and mouth to avoid breathing in.
  • Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat.
  • Do not use on broken skin. Stop use if rash or irritation occurs.
  • Ask a doctor before using if you have kidney disease.
  • KEEP OUT OF REACH OF CHILDREN.
  • USE ONLY AS DIRECTED, INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.

WARNINGS SECTION

Warnings

  • FLAMMABLE, DO NOT USE NEAR HEAT, FLAME OR WHILE SMOKING. CAN CAUSE SERIOUS INJURY OR DEATH.
  • Keep away from face and mouth to avoid breathing in.
  • Avoid spraying in eyes. Contents under pressure. Do not puncture or incinerate. Do not expose to heat or store at temperatures above 120°F/50°C or in enclosed places that could overheat.
  • Do not use on broken skin. Stop use if rash or irritation occurs.
  • Ask a doctor before using if you have kidney disease.
  • KEEP OUT OF REACH OF CHILDREN.
  • USE ONLY AS DIRECTED, INTENTIONAL MISUSE BY DELIBERATELY CONCENTRATING AND INHALING THE CONTENTS CAN BE HARMFUL OR FATAL.

DOSAGE & ADMINISTRATION SECTION

Directions apply to underarms only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Powder and Petals 3.8 ozPowder and Petals 3.8 oz

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83711-142-38Suave Dry Antiperspirant Deodorant Powder and Petals107 g in 1 BOTTLE, SPRAYSPRAY1074

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
83711-14283711-142-38

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROFLUOROCARBON 152A0B1U8K2ME0IACT
CYCLOPENTASILOXANE0THT5PCI0RIACT
PROPANET75W9911L6IACT
PPG-14 BUTYL ETHERR199TJT95TIACT
BUTANE6LV4FOR43RIACT
ISOBUTANEBXR49TP611IACT
FRAGRANCE FLORAL ORC0902236R66Z4YW3X0IACT
DISTEARDIMONIUM HECTORITEX687XDK09LIACT
PROPYLENE CARBONATE8D08K3S51EIACT
BHT1P9D0Z171KIACT
CINNAMYL ALCOHOLSS8YOP444FIACT
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
Suave Dry Antiperspirant Deodorant Powder and PetalsDRY SPRAY ANTIPERSPIRANT DEODORANTSuave Brands Co, LLC41af8db7-7a7b-07b9-e063-6394a90a79fa2026-03-26WarningsExact identifier
ndc (package): 83711-142-38
ndc (product): 83711-142
ndc11 (package): 83711014238
spl id: 4df1d1b6-a91d-5522-e063-6394a90ae48c
spl set id: 41af8db7-7a7b-07b9-e063-6394a90a79fa

Reported adverse events (FAERS/openFDA)#

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