IMPLAHEAL P.OCREAM- illite, acetyl glucosamine, dimethyl sulfon cream

IMPLAHeal P.OCream by

Drug Labeling and Warnings

IMPLAHeal P.OCream by is a Otc medication manufactured, distributed, or labeled by Threedayslove Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

illite, acetyl glucosamine, dimethyl sulfone, hydrolyzed sponge, morinda citrifolia extract,

Olea Europaea (Olive) Fruit Oil
Lavandula Angustifolia (Lavender) Oil
Pinus Sylvestris Leaf Oil
Cananga Odorata Flower Oil
Rosmarinus Officinalis (Rosemary) Leaf Oil
Artemisia Vulgaris Oil
Pelargonium Graveolens Flower Oil
Melaleuca Alternifolia (Tea Tree)Leaf Oil

INACTIVE INGREDIENT

Water
Glycerin
Ceramide 3
Hydrogenated Lecithin
Cyclopentasiloxane
Dimethiconol

etc

PURPOSE

to penetrate into skin deeply and helps improvement

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

INDICATIONS & USAGE

after getting proper amount, let absorption to the improved part by massage

WARNINGS

Warning: 1. Do not use if you have any of following problems during use: ① Rash, red spots, swelling, irritation ② If the application site has any of the above problems due to direct sunlight

2. Precautions for storage and handling ① Close the cap after use ② Keep out of reach of children ③ Do not store under high or low temperature and direct sunlight.

If you continue to use the product, the symptoms may worsen. Stop use and ask a doctor if abnormality occurs.

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

IMPLAHEAL P.OCREAM 
illite, acetyl glucosamine, dimethyl sulfon cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72368-0007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
N-ACETYLGLUCOSAMINE (UNII: V956696549) (N-ACETYLGLUCOSAMINE - UNII:V956696549)	N-ACETYLGLUCOSAMINE	2 g  in 100 mL
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
WATER (UNII: 059QF0KO0R)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72368-0007-1	80 mL in 1 TUBE; Type 0: Not a Combination Product	12/16/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/16/2019

Labeler - Threedayslove Co., Ltd. (693724138)

Registrant - Threedayslove Co., Ltd. (693724138)

Establishment
Name	Address	ID/FEI	Business Operations
Threedayslove Co., Ltd.		693724138	manufacture(72368-0007) , pack(72368-0007) , label(72368-0007)