ZENOL POWERFULX RECOVERYCREAM

Manufacturer
Powerful X
Effective date
2018-08-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:56:41

Label at a glance#

ProductZENOL POWERFULX RECOVERYCREAM
Active ingredientSTEARIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Stearic Acid

INACTIVE INGREDIENT SECTION

Water, Butylene Glycol, etc

OTC - PURPOSE SECTION

Warm up pre/after-execise and after shower

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children


WARNINGS SECTION

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 SECTION

for external use only


INDICATIONS & USAGE SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
70042-0001-12020-01-31C16284748780-19d75b9d1-125a-f424-e053-dadaa90a57ceDrug Facts
70042-0001-22020-01-31C16284748780-19d75b9d1-125a-f424-e053-dadaa90a57ceDrug Facts
70042-0001-32020-01-31C16284748780-19d75b9d1-125a-f424-e053-dadaa90a57ceDrug Facts
70042-0001-42020-01-31C16284748780-19d75b9d1-125a-f424-e053-dadaa90a57ceDrug Facts
70042-0001-52020-01-31C16284748780-19d75b9d1-125a-f424-e053-dadaa90a57ceDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70042-0001-1ZENOL POWERFULX RECOVERYCREAM30 mL in 1 TUBECREAM302
70042-0001-2ZENOL POWERFULX RECOVERYCREAM60 mL in 1 TUBECREAM602
70042-0001-3ZENOL POWERFULX RECOVERYCREAM100 mL in 1 TUBECREAM1002
70042-0001-4ZENOL POWERFULX RECOVERYCREAM250 mL in 1 TUBECREAM2502
70042-0001-5ZENOL POWERFULX RECOVERYCREAM500 mL in 1 BOTTLE, PUMPCREAM5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70042-0001ZENOL POWERFULX RECOVERYCREAM (STEARIC ACID) CREAM [POWERFUL X]2Legacy NDC, 5 package rows20180829_643580b9-a696-5afc-e053-2991aa0a367e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70042-000170042-0001-1, 70042-0001-2, 70042-0001-3, 70042-0001-4, 70042-0001-5

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
STEARIC ACID4ELV7Z65APACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
748da2d5-de52-1054-e053-2991aa0aec0f643580b9-a696-5afc-e053-2991aa0a367e2018-08-29WarningsExact identifier
spl id: 748da2d5-de52-1054-e053-2991aa0aec0f
spl set id: 643580b9-a696-5afc-e053-2991aa0a367e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.