DOCTOR PLUS- stearic acid cream

Doctor Plus by

Drug Labeling and Warnings

Doctor Plus by is a Otc medication manufactured, distributed, or labeled by Powerful X. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Stearic Acid

INACTIVE INGREDIENT

Water, Butylene Glycol, etc

PURPOSE

Warm up pre-execise and after shower

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

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

INDICATIONS & USAGE

Put on the cream and massage your body parts for 10 minutes to warm up before doing exercise.

Apply cream and massge when applying for warm-sensation after shower.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DOCTOR PLUS 
stearic acid cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70042-6001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
STEARIC ACID (UNII: 4ELV7Z65AP) (STEARIC ACID - UNII:4ELV7Z65AP)	STEARIC ACID	1.5 g  in 100 mL

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

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 70042-6001-1	100 mL in 1 TUBE; Type 0: Not a Combination Product	01/09/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		01/09/2018

Labeler - Powerful X (689515038)

Registrant - Powerful X (689515038)

Establishment
Name	Address	ID/FEI	Business Operations
Powerful X		689515038	manufacture(70042-6001) , label(70042-6001) , pack(70042-6001)