Home NDC 70042-0007-4 PowerfulX RecoveryCream
Product NDC 70042-0007
Requested package NDC 70042-0007-4
11-digit product format 700420007
Labeler code 70042
Product ID 70042-0007_2b52a447-dd5c-1baf-e063-6294a90ad5c4
Type HUMAN OTC DRUG
Nonproprietary name Acetyl Glucosamine, Dimethyl Sulfone
Dosage form CREAM
Route TOPICAL
Labeler Power Fulx Co., Ltd.
Marketing category UNAPPROVED DRUG OTHER
Marketing start 2024-12-25
Substance DIMETHYL SULFONE; N-ACETYLGLUCOSAMINE
Active strength .02; .02 g/100mL; g/100mL
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base PowerfulX RecoveryCream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength DIMETHYL SULFONE .02 g/100mL N-ACETYLGLUCOSAMINE .02 g/100mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 9H4PO4Z4FT Internal UNII lookup V956696549 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70042-0007-1 PowerfulX RecoveryCream 500 mL in 1 BOTTLE, PUMP CREAM 500 5 70042-0007-2 PowerfulX RecoveryCream 250 mL in 1 TUBE CREAM 250 5 70042-0007-3 PowerfulX RecoveryCream 100 mL in 1 TUBE CREAM 100 5 70042-0007-4 PowerfulX RecoveryCream 60 mL in 1 TUBE CREAM 60 5 70042-0007-5 PowerfulX RecoveryCream 30 mL in 1 TUBE CREAM 30 5 70042-0007-6 PowerfulX RecoveryCream 2 mL in 1 JAR CREAM 2 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70042-0007 POWERFULX RECOVERYCREAM (ACETYL GLUCOSAMINE, DIMETHYL SULFONE) CREAM [POWER FULX CO., LTD.] 5 Current NDC, 6 package rows 20250117_2b5213b0-8c05-dd2b-e063-6394a90a8bfe.zip
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.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 70042-0007-4 70042000704 60 mL in 1 TUBE (70042-0007-4) 60 ml 2024-12-25 No No Current