SWEATBLOCK Antiperspirant Lotion for Hands & Feet

Manufacturer
DC Alpine Partners, LLC
Effective date
2022-01-01
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-01 22:19:41

Label at a glance#

ProductSWEATBLOCK
Active ingredientALUMINUM SESQUICHLOROHYDRATE
Label structure13 sections

Dosage and administration

Wash and dry hands/feet thoroughly before applying. For hands: Apply a pearl-sized amount to palm, then rub palms together for 15-20 seconds. For feet: Apply a small amount to both feet and massage into skin until evenly dispersed. Tip for Success: For the first 4 weeks, apply nightly before bed and at least 2 times per day. After that, apply as needed. The more you use SweatBlock, the more effective it can be.

Label contents#

Full prescribing information#

SWEATBLOCK

SPL UNCLASSIFIED SECTION

Antiperspirant Lotion for Hands & Feet

PERFECT FOR

Excessive Sweating and Hyperhidrosis

Confident Handshaking and Hand Holding

Nervous Sweating

Professionals

Gamers

Athletes and Weight Lifters

HOW TO USE

INSTRUCTIONS FOR USE SECTION

1. WASH + DRY

Wash and dry hands or feet before applying SweatBlock lotion.

2. APPLY

For hands, Apply a pearl-sized amount to one palm. For Feet, Apply a small amount to each foot.

3. RUB IN LOTION FOR 15 SECONDS

For hands, rub palms together for 10-15 seconds until lotion is fully absorbed. For feet, rub into skin until lotion is evenly dispersed and absorbed. Wash hands after foot application.

LOVE IT... OR IT'S FREE!

SPL UNCLASSIFIED SECTION

If SweatBlock doesn't keep you dry, it's free! Learn more about our 30-day money back guarantee at

www.sweatblock.com/guarantee

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Sesquichlorohydrate (20%)

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Use

INDICATIONS & USAGE SECTION

  • Reduces perspiration

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

on broken or irritated skin.

Stop use if

OTC - STOP USE SECTION

rash or irritation occurs.

Ask a doctor before use if

OTC - ASK DOCTOR SECTION

you have kidney disease.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

  • Wash and dry hands/feet thoroughly before applying.
  • For hands: Apply a pearl-sized amount to palm, then rub palms together for 15-20 seconds.
  • For feet: Apply a small amount to both feet and massage into skin until evenly dispersed.
  • Tip for Success: For the first 4 weeks, apply nightly before bed and at least 2 times per day. After that, apply as needed. The more you use SweatBlock, the more effective it can be.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Caprylic/Capric Triglyceride, Cetearyl Alcohol, Glyceryl Stearate, PEG-100 Stearate, Butylene Glycol, Cyclopentasiloxane, Glycerin, Dimethicone, Steareth-2, Steareth-21, Phenoxyethanol, Hordeum Distichon (Barley) Extract, Caprylyl Glycol, Phellodendron Amurense Bark Extract, Santalum Album (Sandalwood) Extract, Chlorphenesin, Tetrasodium Glutamate Diacetate, Sodium Hyaluronate, Glycolipids, Tocopherol, Soybean Phytosterols, Aloe Barbadensis Leaf Juice

Questions?

OTC - QUESTIONS SECTION

Call toll free 1-855-796-2566

Distributed by

SPL UNCLASSIFIED SECTION

SweatBlock - Alpine, UT 84004

Made with (heart symbol) in the USA

Stay Confident Longer TM

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

SWEATBLOCK

Antiperspirant Lotion for HANDS & FEET

50ml (1.69 fl oz)

SweatBlock Antiperspirant Lotion for Hands & Feet Labels

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54913-20054913-200-50

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 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
d4807a52-d414-07cc-e053-2995a90a53e07d553698-faa1-155d-e053-2991aa0a7bb32022-01-01WarningsExact identifier
spl id: d4807a52-d414-07cc-e053-2995a90a53e0
spl set id: 7d553698-faa1-155d-e053-2991aa0a7bb3

Reported adverse events (FAERS/openFDA)#

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