lumoe skin1 skin remedy

Generic: kali muriaticum, prunus spinosa, silicea, sarsaparilla

Labeler: applied bioenergetics, llc
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name lumoe skin1 skin remedy
Generic Name kali muriaticum, prunus spinosa, silicea, sarsaparilla
Labeler applied bioenergetics, llc
Dosage Form TABLET, CHEWABLE
Routes
ORAL
Active Ingredients

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

Manufacturer
Applied Bioenergetics, LLC

Identifiers & Regulatory

Product NDC 81425-007
Product ID 81425-007_507e1913-f6b0-4693-a99c-77d080e68294
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2024-09-27

Pharmacologic Class

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]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 81425007
Hyphenated Format 81425-007

Supplemental Identifiers

UNII
660YQ98I10 53Y84VPS2W ETJ7Z6XBU4 2H1576D5WG

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lumoe skin1 skin remedy (source: ndc)
Generic Name kali muriaticum, prunus spinosa, silicea, sarsaparilla (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12 [hp_C]/1
  • 30 [hp_C]/1
source: ndc
Packaging
  • 180 TABLET, CHEWABLE in 1 BOTTLE (81425-007-10)
source: ndc

Packages (1)

81425-007-10 180 TABLET, CHEWABLE in 1 BOTTLE (81425-007-10)

Ingredients (4)

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)

Linked Drug Pages (1)

LUMOe SKIN1 Skin Remedy ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "507e1913-f6b0-4693-a99c-77d080e68294", "openfda": {"unii": ["660YQ98I10", "53Y84VPS2W", "ETJ7Z6XBU4", "2H1576D5WG"], "spl_set_id": ["d4d7fd2f-66bf-407d-ad36-2462e880b9f5"], "manufacturer_name": ["Applied Bioenergetics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, CHEWABLE in 1 BOTTLE (81425-007-10)", "package_ndc": "81425-007-10", "marketing_start_date": "20240927"}], "brand_name": "LUMOe SKIN1 Skin Remedy", "product_id": "81425-007_507e1913-f6b0-4693-a99c-77d080e68294", "dosage_form": "TABLET, CHEWABLE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]", "Potassium Compounds [CS]", "Potassium Salt [EPC]"], "product_ndc": "81425-007", "generic_name": "Kali muriaticum, Prunus spinosa, Silicea, Sarsaparilla", "labeler_name": "Applied Bioenergetics, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LUMOe SKIN1 Skin Remedy", "active_ingredients": [{"name": "POTASSIUM CHLORIDE", "strength": "12 [hp_C]/1"}, {"name": "PRUNUS SPINOSA FLOWER BUD", "strength": "30 [hp_C]/1"}, {"name": "SILICON DIOXIDE", "strength": "30 [hp_C]/1"}, {"name": "SMILAX ORNATA ROOT", "strength": "30 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20240927", "listing_expiration_date": "20261231"}