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ZENOL POWERFULX RECOVERYCREAM

Medically reviewed on February 1, 2018

Dosage form: cream
Ingredients: STEARIC ACID 1.5g in 100mL
Labeler: Flexpoweraws
NDC Code: 70042-0001

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.

Drug Facts

Stearic Acid

Water, Butylene Glycol, etc

Warm up pre/after-execise and after shower

keep out of reach of the children


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

for external use only


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.

ZENOL POWERFULX RECOVERYCREAM 
stearic acid cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70042-0001
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
STEARIC ACID (STEARIC ACID) STEARIC ACID1.5 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
BUTYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:70042-0001-130 mL in 1 TUBE
2NDC:70042-0001-260 mL in 1 TUBE
3NDC:70042-0001-3100 mL in 1 TUBE
4NDC:70042-0001-4250 mL in 1 TUBE
5NDC:70042-0001-5500 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other02/02/2018
Labeler - Flexpoweraws (689515038)
Registrant - Flexpoweraws (689515038)
Establishment
NameAddressID/FEIOperations
Flexpoweraws689515038manufacture(70042-0001), label(70042-0001), pack(70042-0001)

 
Flexpoweraws

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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