83472-801 Lacto powder cleanser

Lacto powder cleanser by

Drug Labeling and Warnings

Lacto powder cleanser by is a Otc medication manufactured, distributed, or labeled by Y2K Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

LACTO POWDER CLEANSER- sodium lauroyl glutamate, sodium cocoyl glycinate powder 
Y2K Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

----------

83472-801 Lacto powder cleanser

Active Ingredients

Allantoin 5%
Ascorbic Acid 0.0006%

Purposes

Sodium Lauroyl Glutamate 22.89% ----------------------------- remove dirt and impurities
Sodium Cocoyl Glycinate 17.09% ------------------------------- deep cleanse

Uses

remove impurities and dead skin cells @ balance oil and water content to keep healthy skin

Warnings

For external use only

Warnings

Do not use on damaged or broken skin

Warnings

When using this product keep out of eyes. Rinse with water to remove.

Warnings

Stop use and ask a doctor if rash occurs

Warnings

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Dispense a small amount of powder into the dry palms, add a moderate amount of water to create a lather, massage lightly over the face, and rinse thoroughly with lukewarm water.

Other information

@protect the product in this container from excessive heat and direct sun

Inactive ingredients

Microcrystalline Cellulose, D-Glucose, Allantoin, Betaine, Sodium Cocoyl Isethionate, Mannitol, Ethylcellulose, Silica, Lactobacillus Ferment Lysate, Maltodextrin, Astaxanthin, Sodium Starch Octenylsuccinate, Acacia Senegal Gum, 1,2-Hexanediol, Papain, Tocopherol, Ascorbic Acid

Label

Lacto Cleanser

LACTO POWDER CLEANSER 
sodium lauroyl glutamate, sodium cocoyl glycinate powder

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83472-801
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ASCORBIC ACID (UNII: PQ6CK8PD0R) (ASCORBIC ACID - UNII:PQ6CK8PD0R)	ASCORBIC ACID	0.0006 g  in 100 g
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
MANNITOL (UNII: 3OWL53L36A)
ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
ASTAXANTHIN (UNII: 8XPW32PR7I)
TOCOPHEROL (UNII: R0ZB2556P8)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
PAPAIN (UNII: A236A06Y32)
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
BETAINE (UNII: 3SCV180C9W)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
LIMOSILACTOBACILLUS FERMENTUM (UNII: 2C1F12C6AP)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
ACACIA (UNII: 5C5403N26O)
SODIUM LAUROYL GLUTAMATE (UNII: NCX1UU2D33)
SODIUM COCOYL ISETHIONATE (UNII: 518XTE8493)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83472-801-02	50 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	11/10/2023
2	NDC: 83472-801-20	1 g in 1 POUCH; Type 0: Not a Combination Product	11/10/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/10/2023	01/08/2024

Labeler - Y2K Co., Ltd. (695705051)

Revised: 1/2024

Document Id: 0e677251-f959-bf8d-e063-6394a90af9c4

34390-5

Set id: 09c84db0-b315-c084-e063-6394a90a0215

Version: 4

Effective Time: 20240107