NICK RELIEF

Dosage form: stick
Ingredients: ALUMINUM SULFATE 46mg in 1mL
Labeler: 220 LABORATORIES INC
NDC code: 57367-007

Medically reviewed by Drugs.com. Last updated on Feb 23, 2024.

NICK RELIEF PACKAGING

Warnings: For external use only. Flammable product.
Do not use in or around eyes or sensitive areas.
Discontinue use and consult a doctor if bleeding persists.

Directions:
Apply cold water to area and pat dry.
Shake Nick Relief.
Apply gently to area.
Rinse applicator head with warm water after each use.

Uses:
Stops bleeding from minor nicks and cuts.
No stinging or skin irritation.
Helps to speed healing.

Active Ingredient: Aluminum Sulfate 46%

Inactive ingredients: Witch Hazel Distillate, Water (Aqua), Propylene Glycol, Panthenol, Horsetail (Equisetum Arvense) Extract, Passionflower (Passiflora Incarnata) Fruit Extract, Diazolidinyl Urea, Methylparaben, Propylparaben

KEEP OUT OF REACH OF CHILDREN

Purpose: Stops bleeding

Clubman

Nick Relief

For razor nicks and cuts

Stops Bleeding Instantly

NICK RELIEF
aluminum sulfate stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57367-007
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SULFATE (ALUMINUM CATION)	ALUMINUM SULFATE	46 mg in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER
WITCH HAZEL
PROPYLENE GLYCOL
DIAZOLIDINYLUREA
PANTHENOL
METHYLPARABEN
PROPYLPARABEN
MELISSA OFFICINALIS
MATRICARIA RECUTITA
ALOE VERA LEAF
GERANIUM EXTRACT
QUERCUS ALBA
ROSA CANINA FRUIT
SAGE
COMFREY
YARROW FLOWER
EAST INDIAN LEMONGRASS OIL
.ALPHA.-TOCOPHEROL ACETATE, D-

Packaging
#	Item Code	Package Description
1	NDC:57367-007-20	1 APPLICATOR (APPLICATOR) in 1 BLISTER PACK
1	NDC:57367-007-07	7 mL in 1 APPLICATOR

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part347	11/27/1997

Labeler - 220 LABORATORIES INC (783247950)

Registrant - 220 LABORATORIES INC (783247950)

Establishment
Name	Address	ID/FEI	Operations
220 LABORATORIES INC		783247950	manufacture

Revised: 03/2010

Document Id: f82e9fcf-7441-4beb-8f64-79b6b8ee5061

Set id: e3d78fda-a380-4f78-b5f9-efb3c2f0e1dc

Version: 2

Effective Time: 20100304

220 LABORATORIES INC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer