SPAREDI MINT AND EUCALYPTUS MASK- benzalkonium chloride cream
CHEMCO CORPORATION

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.

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49283-101-07

Benzalkonium chloride 0.1%

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.

For external use only.

•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.

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

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

MINT CREAM MASK 07

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

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

Ingredient Name	Strength
Inactive Ingredients
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

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

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

Labeler - CHEMCO CORPORATION (032495954)

Registrant - CHEMCO CORPORATION (032495954)

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