SWEATBLOCK- aluminum chloride solution

SWEATBLOCK by

Drug Labeling and Warnings

SWEATBLOCK by is a Otc medication manufactured, distributed, or labeled by DC Alpine Partners, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SAFE & EFFECTIVE

• Reduce sweating and restore confidence
• Up to 7-days of protection per use*
• Doctor recommended

​

CLINICAL STRENGTH

Drug Facts

Active ingredient

Aluminum chloride 14%

Purpose

Antiperspirant

Uses

• Decreases underarm sweating
• Reduces excessive sweating

Warnings

For external use only.

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.

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

Directions

Apply at bedtime. Ensure skin is clean and dry. Use every 7 days or as needed.

Inactive ingredients

Water, botanical extracts, polyethylene glycol 8000, polysorbate 20, vitamin E oil, eugenol.

Questions?

Call Toll Free 1-855-796-2566

SWEATBLOCK Usage Instructions:

1. Apply at bedtime.

2. Dab on clean, dry skin. (do not rub)

3. Air dry for 5 min. and go to bed.
4. In the morning, wash treatred area with soap.

Want to know more?

www.sweatblock.com

Distributed by

SweatBlock - Alpine, UT 84004

Made in the USA

SWEATBLOCK Clinical Strength Antiperspirant

SWEATBLOCK

CLINICAL STRENGTH

Sweat Less. Live More. (TM)

CLINICAL STRENGTH

10 sweat wipes

SWEATBLOCK

Antiperspirant Wipes

Up to Seven Days 7 Protection Per Use*

Doctor Trusted.

Doctor Recommended.

*Consumer perception reports support the appearance of dryness for up to 7 days per use. Individual results may vary.

SWEATBLOCK Clinical Strength Antiperspirant Labels

INGREDIENTS AND APPEARANCE

SWEATBLOCK 
aluminum chloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 54913-001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM CHLORIDE (UNII: 3CYT62D3GA) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM CHLORIDE	140 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
EUGENOL (UNII: 3T8H1794QW)
POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 54913-001-10	10 in 1 BOX	12/29/2019
1		2.6 mL in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part350	12/29/2019

Labeler - DC Alpine Partners, LLC (042895991)