FDA.reportPublic FDA data

Hi and Dri Antiperspirant Roll On

Manufacturer
Revlon Consumer Products Corp | REVLON, INC.
Effective date
2024-12-31
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:49:50

Label at a glance#

ProductHi and Dri Antiperspirant Roll On
Active ingredientALUMINUM CHLOROHYDRATE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Aluminum chlorohydrate 18%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

WARNINGS SECTION

Warnings:

For external use only.

Do not use on broken skin

Ask a doctor before use if you have kidney disease

Stop use if rash or irriation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

INACTIVE INGREDIENT SECTION

Inactive Ingredients

aqua((water) eau), glyceryl stearate, laureth-23, magnesium aluminum silicate, laureth-4, lauric acid, cetearyl alcohol, behentrimonium methosulfate, edta

INDICATIONS & USAGE SECTION

Reduces underarm wetness

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hi & Dri Roll-On AntiperspirantHi & Dri Roll-On AntiperspirantHi & Dri Roll-On Antiperspirant

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Hi and DriHi and Dri

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10967-787-17Hi and Dri Antiperspirant Roll On50 mL in 1 BOTTLE, WITH APPLICATORLIQUID501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10967-787HI AND DRI ANTIPERSPIRANT ROLL ON (ALUMINUM CHLOROHYDRATE) LIQUID [REVLON CONSUMER PRODUCTS CORP]1Current NDC, 1 package rows20250101_2a99e9e8-3d17-ee0b-e063-6294a90ae4ef.zip

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-78710967-787-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
MAGNESIUM ALUMINUM SILICATE6M3P64V0NCIACT
LAURETH-46HQ855798JIACT
LAURIC ACID1160N9NU9UIACT
CETEARYL ALCOHOL2DMT128M1SIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
EDTA9G34HU7RV0IACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
LAURETH-23N72LMW566GIACT
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
Hi and Dri Antiperspirant Roll OnALUMINUM CHLOROHYDRATERevlon Consumer Products Corp2a99e9e8-3d17-ee0b-e063-6294a90ae4ef2024-12-31WarningsExact identifier
ndc (package): 10967-787-17
ndc (product): 10967-787
ndc11 (package): 10967078717
spl id: 2a99c981-daf3-71e5-e063-6294a90a5c1d
spl set id: 2a99e9e8-3d17-ee0b-e063-6294a90ae4ef

Reported adverse events (FAERS/openFDA)#

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