Home NDC 81425-007 LUMOe SKIN1 Skin Remedy
Product NDC 81425-007
11-digit product format 814250007
Labeler code 81425
Product ID 81425-007_507e1913-f6b0-4693-a99c-77d080e68294
Type HUMAN OTC DRUG
Nonproprietary name Kali muriaticum, Prunus spinosa, Silicea, Sarsaparilla
Dosage form TABLET, CHEWABLE
Route ORAL
Labeler Applied Bioenergetics, LLC
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2024-09-27
Substance POTASSIUM CHLORIDE; PRUNUS SPINOSA FLOWER BUD; SILICON DIOXIDE; SMILAX ORNATA ROOT
Active strength 12; 30; 30; 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
Pharmacologic classes Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base LUMOe SKIN1 Skin Remedy
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength POTASSIUM CHLORIDE 12 [hp_C]/1 PRUNUS SPINOSA FLOWER BUD 30 [hp_C]/1 SILICON DIOXIDE 30 [hp_C]/1 SMILAX ORNATA ROOT 30 [hp_C]/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 4 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 81425-007-10 LUMOe SKIN1 Skin Remedy 180 in 1 BOTTLE TABLET, CHEWABLE 180 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 81425-007 LUMOE SKIN1 SKIN REMEDY (KALI MURIATICUM, PRUNUS SPINOSA, SILICEA, SARSAPARILLA) TABLET, CHEWABLE [APPLIED BIOENERGETICS, LLC] 1 Current NDC, 1 package rows 20241009_d4d7fd2f-66bf-407d-ad36-2462e880b9f5.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 Marketing start Sample Exclude flag Status 81425-007-10 81425000710 180 TABLET, CHEWABLE in 1 BOTTLE (81425-007-10) 2024-09-27 No No Current