NICK RELIEF

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

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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 TypeHUMAN OTC DRUGItem Code (Source)NDC:57367-007
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALUMINUM SULFATE (ALUMINUM CATION) ALUMINUM SULFATE46 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
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 CodePackage Description
1NDC:57367-007-201 APPLICATOR (APPLICATOR) in 1 BLISTER PACK
1NDC:57367-007-077 mL in 1 APPLICATOR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart34711/27/1997
Labeler - 220 LABORATORIES INC (783247950)
Registrant - 220 LABORATORIES INC (783247950)
Establishment
NameAddressID/FEIOperations
220 LABORATORIES INC783247950manufacture

Revised: 03/2010
 
220 LABORATORIES INC

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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