ARRID XX Roll On

Manufacturer
Church & Dwight Co., Inc. | Church & Dwight Canada Corp
Effective date
2020-09-03
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 23:16:17

Label at a glance#

ProductARRID XX Roll On Antiperspirant Deodorant Regular
Active ingredientALUMINUM CHLOROHYDRATE
Label structure9 sections

Dosage and administration

Shake gently. Apply a thin layer to underarms only.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Chlorohydrate (16%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

reduces underarm perspiration

Warnings For external use only

WARNINGS SECTION

Do not use on broken skin

Stop use if rash or irritation occurs

Ask a doctor before use if you have kidney disease

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Shake gently. Apply a thin layer to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Steareth-2, Steareth-21, Dimethicone, Allantoin, Fragrance.

Questions

OTC - QUESTIONS SECTION

? 1-800-524-1328 M-F 9-5 ET www.arrid.com

Principal Display

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW LOOK!

ARRID
EXTRA EXTRA DRY

XX

Regular

ROLL-ON

ANTIPERSPIRANT

DEODORANT

MAXIMUM

STRENGTH

PROTECTION


NET WT. 2.5 FL. OZ. (74mL)

ARLBF-05062-10_70504553_DA1079173ARLBF-05062-10_70504553_DA1079173

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10237-901-252020-09-03C16284748780-19d75b9cf-d556-f424-e053-dadaa90a57ceARRID XX Roll On Antiperspirant Deodorant
10237-901-252020-01-31C16284748780-19d75b9cf-d556-f424-e053-dadaa90a57ceARRID XX Roll On Antiperspirant Deodorant

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ALUMINUM CHLOROHYDRATEACTIVE INGREDIENTHPN8MZW13M2
ALUMINUM CHLOROHYDRATEACTIVE MOIETYHPN8MZW13M2
ALLANTOININACTIVE INGREDIENT344S277G0Z2
DIMETHICONEINACTIVE INGREDIENT92RU3N3Y1O2
STEARETH-2INACTIVE INGREDIENTV56DFE46J52
STEARETH-21INACTIVE INGREDIENT53J3F32P582
WATERINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10237-90110237-901-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 7 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
STEARETH-2STEARETH-2V56DFE46J5AEROSOL, FOAM / TOPICAL1.09 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-21STEARETH-2153J3F32P58CREAM / TOPICAL3 %w/wExact identifier — unii candidate
2 equally ranked IID candidates
STEARETH-21STEARETH-2153J3F32P58LOTION / TOPICAL3 %w/wExact identifier — unii candidate
2 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5LOTION / TOPICAL0.4 %w/wExact identifier — unii candidate
4 equally ranked IID candidates
ALLANTOINALLANTOIN344S277G0ZGEL / TOPICAL8 mgExact identifier — unii candidate
STEARETH-2STEARETH-2V56DFE46J5CREAM / TOPICAL643 mgExact identifier — unii candidate
4 equally ranked IID candidates
STEARETH-2STEARETH-2V56DFE46J5OINTMENT / TOPICAL714 mgExact identifier — unii candidate
4 equally ranked IID candidates

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
ae6a0521-7e68-89bd-e053-2a95a90a3fdfc1bb2120-5854-4f4a-9d55-4d707bd1ebf22020-09-03WarningsExact identifier
spl id: ae6a0521-7e68-89bd-e053-2a95a90a3fdf
spl set id: c1bb2120-5854-4f4a-9d55-4d707bd1ebf2

Reported adverse events (FAERS/openFDA)#

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