NICK RELIEF- aluminum sulfate stick

NICK RELIEF by

Drug Labeling and Warnings

NICK RELIEF by is a Otc medication manufactured, distributed, or labeled by 220 LABORATORIES INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BOXED WARNING

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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.

DOSAGE & ADMINISTRATION

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.

INDICATIONS & USAGE

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

ACTIVE INGREDIENT

Active Ingredient: Aluminum Sulfate 46%

INACTIVE INGREDIENT

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

KEEP OUT OF REACH OF CHILDREN

PURPOSE

Purpose: Stops bleeding

PRINCIPAL DISPLAY PANEL

Clubman

Nick Relief

For razor nicks and cuts

Stops Bleeding Instantly

INGREDIENTS AND APPEARANCE

NICK RELIEF 
aluminum sulfate stick

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

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALUMINUM SULFATE (UNII: 34S289N54E) (ALUMINUM CATION - UNII:3XHB1D032B)	ALUMINUM SULFATE	46 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
WITCH HAZEL (UNII: 101I4J0U34)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
DIAZOLIDINYLUREA (UNII: H5RIZ3MPW4)
PANTHENOL (UNII: WV9CM0O67Z)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
MELISSA OFFICINALIS (UNII: YF70189L0N)
MATRICARIA RECUTITA (UNII: G0R4UBI2ZZ)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
GERANIUM EXTRACT (UNII: 6H429I0Y3L)
QUERCUS ALBA (UNII: XR6BC2ZUAM)
ROSA CANINA FRUIT (UNII: 3TNW8D08V3)
SAGE (UNII: 065C5D077J)
COMFREY (UNII: D05HXK6R3G)
YARROW FLOWER (UNII: YQR8R0SQEA)
EAST INDIAN LEMONGRASS OIL (UNII: UP0M8M3VZW)
.ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 57367-007-20	1 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	Business Operations
220 LABORATORIES INC		783247950	manufacture