POWERFULX RECOVERYCREAM- acetyl glucosamine, dimethyl sulfone cream

PowerfulX RecoveryCream by

Drug Labeling and Warnings

PowerfulX RecoveryCream by is a Otc medication manufactured, distributed, or labeled by Power Fulx Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Dimethyl Sulfone, N-Acetylglucosamine

INACTIVE INGREDIENT

Water, Butylene Glycol, etc

PURPOSE

Effection : Recovery and pain relief of minor aches and pains of muscles and joints

KEEP OUT OF REACH OF CHILDREN

keep out of reach of the children

WARNINGS

• Warnings : For external use only: avoiding the face and eye areas.

DOSAGE & ADMINISTRATION

Uses : For the temporary relief of minor aches and pains of muscles and joints

INDICATIONS & USAGE

Directions :

ㆍApply a proper amount of this product to skin 10 minutes before exercise.

ㆍAfter shower, apply to skin and massage.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POWERFULX RECOVERYCREAM 
acetyl glucosamine, dimethyl sulfone cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 70042-0007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	0.02 g  in 100 mL
N-ACETYLGLUCOSAMINE (UNII: V956696549) (N-ACETYLGLUCOSAMINE - UNII:V956696549)	N-ACETYLGLUCOSAMINE	0.02 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: 70042-0007-1	500 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/25/2024
2	NDC: 70042-0007-2	250 mL in 1 TUBE; Type 0: Not a Combination Product	12/25/2024
3	NDC: 70042-0007-3	100 mL in 1 TUBE; Type 0: Not a Combination Product	12/25/2024
4	NDC: 70042-0007-4	60 mL in 1 TUBE; Type 0: Not a Combination Product	12/25/2024
5	NDC: 70042-0007-5	30 mL in 1 TUBE; Type 0: Not a Combination Product	12/25/2024
6	NDC: 70042-0007-6	2 mL in 1 JAR; Type 0: Not a Combination Product	12/25/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		12/25/2024

Labeler - Power Fulx Co., Ltd. (963407605)

Registrant - Power Fulx Co., Ltd. (963407605)

Establishment
Name	Address	ID/FEI	Business Operations
Power Fulx Co., Ltd.		963407605	manufacture(70042-0007) , label(70042-0007) , pack(70042-0007)