SPAREDI MINT AND EUCALYPTUS MASK- benzalkonium chloride cream

SPAREDI MINT AND EUCALYPTUS MASK by

Drug Labeling and Warnings

SPAREDI MINT AND EUCALYPTUS MASK by is a Otc medication manufactured, distributed, or labeled by CHEMCO CORPORATION. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Benzalkonium chloride 0.1%

PURPOSE

Antibacterial

USES:

To decrease bacteria on the skin.

DIRECTIONS:

Apply a thin layer to cover the foot. Leave for 10 minutes, then rinse
thoroughly with warm water.

WARNINGS

For external use only.

WHEN USING

Keep out of eyes. In case of contact with eyes, rinse thoroughly
with water. Do not apply to wounds or damaged skin.
Do not apply to the irritated skin or if excessive irritation develops.

KEEP OUT OF REACH OF CHILDREN

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

INACTIVE INGREDIENT

Aqua, Cetyl Alcohol, Stearyl Alcohol, Methyl Salicylate, Eucalyptus Globulus Leaf Oil, DMDM Hydantoin, Methylparaben, Propylparaben, Mentha Piperita (Peppermint) Oil, Sodium Hyaluronate, Sodium PCA, Wheat Amino Acids, Panthenol, Symphytum Officinale (Comfrey) Extract, Hydroxyproline, Cetrimonium Chloride, Argania Spinosa Kernel Oil (Organic), Cocos Nucifera Oil (Organic), FD&C Yellow #5 (CI 19140), FD&C Blue #1 (Cl 42090).

SPAREDI - MINT AND EUCALYPTUS CREAM MASK 0.7 oz

INGREDIENTS AND APPEARANCE

SPAREDI MINT AND EUCALYPTUS MASK 
benzalkonium chloride cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 49283-101
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y)	BENZALKONIUM CHLORIDE	0.1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
ARGANIA SPINOSA WHOLE (UNII: 83K6O4FR76)
EUCALYPTUS GLOBULUS LEAF (UNII: S546YLW6E6)
MENTHA PIPERITA LEAF (UNII: A389O33LX6)
CETYL ALCOHOL (UNII: 936JST6JCN)
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
COCOS NUCIFERA WHOLE (UNII: 245J88W96L)
WATER (UNII: 059QF0KO0R)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
METHYL SALICYLATE (UNII: LAV5U5022Y)
METHYLPARABEN (UNII: A2I8C7HI9T)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
DMDM HYDANTOIN (UNII: BYR0546TOW)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
PANTHENOL (UNII: WV9CM0O67Z)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
SODIUM COCOYL WHEAT AMINO ACIDS (UNII: JW3VT57I11)
HYDROXYPROLINE (UNII: RMB44WO89X)
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y)

Product Characteristics
Color	green	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 49283-101-07	20 g in 1 POUCH; Type 0: Not a Combination Product	01/17/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/17/2023

Labeler - CHEMCO CORPORATION (032495954)

Registrant - CHEMCO CORPORATION (032495954)

Establishment
Name	Address	ID/FEI	Business Operations
CHEMCO CORPORATION		032495954	manufacture(49283-101)