MIRACLE SOS BLACK- moringa oleifera leaf extract, bamboo charcoal powder, soap

MIRACLE SOS BLACK by

Drug Labeling and Warnings

MIRACLE SOS BLACK by is a Otc medication manufactured, distributed, or labeled by Ddoruroo Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Moringa Oleifera Leaf Extract, Bamboo Charcoal Powder

INACTIVE INGREDIENT

Stearic Acid, Myristic Acid, Lauric Acid, etc.

PURPOSE

SKIN PROTECTANT

KEEP OUT OF REACH OF CHILDREN

KEEP OUT OF REACH OF THE CHILDREN

INDICATIONS & USAGE

After make soap bubbles with lukewarm water and then wash the face sofly while massaging the entire face.

WARNINGS

1. Do not use in the following cases(Eczema and scalp wounds)
2.Side Effects
1)Due to the use of this druf if rash, irritation, itching and symptopms of hypersnesitivity occur dicontinue use and consult your phamacisr or doctor
3.General Precautions
1)If in contact with the eyes, wash out thoroughty with water If the symptoms are servere, seek medical advice immediately
2)This product is for exeternal use only. Do not use for internal use
4.Storage and handling precautions
1)If possible, avoid direct sunlight and store in cool and area of low humidity
2)In order to maintain the quality of the product and avoid misuse
3)Avoid placing the product near fire and store out in reach of children

DOSAGE & ADMINISTRATION

for external use only

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MIRACLE SOS BLACK 
moringa oleifera leaf extract, bamboo charcoal powder, soap

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 71484-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MORINGA OLEIFERA LEAF (UNII: 4WET1AWO9B) (MORINGA OLEIFERA LEAF - UNII:4WET1AWO9B)	MORINGA OLEIFERA LEAF	33.8 g  in 100 g
ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10)	ACTIVATED CHARCOAL	0.7 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 71484-0001-1	100 g in 1 CARTON; Type 0: Not a Combination Product	05/01/2017

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		05/01/2017

Labeler - Ddoruroo Co., Ltd. (694209410)

Registrant - Ddoruroo Co., Ltd. (694209410)

Establishment
Name	Address	ID/FEI	Business Operations
Ddoruroo Co., Ltd.		694209410	manufacture(71484-0001) , pack(71484-0001) , label(71484-0001)