Hi and Dri Roll On

Manufacturer
Revlon Consumer Products Corp | REVLON, INC. | Revlon South Africa (PTY) Ltd
Effective date
2016-11-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:21:21

Label at a glance#

ProductHi and Dri 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

FDA-Initiated Inactive NDC Indexing#

Products#

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

DailyMed product names page 1 of 1 · 21 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10967-60010967-600-17
10967-60210967-602-17

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 38 matching rows.

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
2cc6c5dc-c2ed-afa4-e063-6394a90aaedf40f4cc70-6730-44ef-e054-00144ff88e882025-01-28WarningsExact identifier
spl set id: 40f4cc70-6730-44ef-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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