Over-the-counter drug · UNAPPROVED HOMEOPATHIC
LUMOe SKIN1 Skin Remedy NDC 81425-007
kali muriaticum, prunus spinosa, silicea, sarsaparilla · Potassium chloride 12 [hp_C]/1 + 3 more ingredients · Tablet, Chewable · Oral · Applied Bioenergetics, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 81425-007-10 | 8142500071081425000710 | 180 TABLET, CHEWABLE in 1 BOTTLE (81425-007-10)Marketed from Sep 27, 2024 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- LUMOe SKIN1 Skin Remedy
- Generic name (nonproprietary)
- kali muriaticum, prunus spinosa, silicea, sarsaparilla
- Active ingredients
- Potassium chloride — 12 [hp_C]/1Prunus spinosa flower bud — 30 [hp_C]/1Silicon dioxide — 30 [hp_C]/1Smilax ornata root — 30 [hp_C]/1
- Dosage form
- Tablet, Chewable
- Route
- Oral
- Labeler
- Applied Bioenergetics, LLCNDC labeler code 81425
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
- Identifiers
- Product ID 81425-007_507e1913-f6b0-4693-a99c-77d080e68294SPL ID 507e1913-f6b0-4693-a99c-77d080e68294SPL set ID d4d7fd2f-66bf-407d-ad36-2462e880b9f5UNII 660YQ98I10, 53Y84VPS2W, ETJ7Z6XBU4, 2H1576D5WG
- Pharmacologic class
- Osmotic Laxative; Potassium Salt
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N481425000710followed by a unit qualifier and the quantityPackage 81425-0007-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
Indications (excerpt from the label)
Uses* Temporarily Relieves Minor and Occasional Symptoms: • itchy • redness • blemish • headaches • sacral pain • sensitive crusty skin
Excerpt only. Read the full label for complete information.
About NDC 81425-007
- What is NDC 81425-007?
- 81425-007 is the product NDC for LUMOe SKIN1 Skin Remedy, Potassium chloride 12 [hp_C]/1 + 3 more ingredients tablet, chewable, listed with the FDA by Applied Bioenergetics, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- LUMOe SKIN1 Skin Remedy (Kali muriaticum, Prunus spinosa, Silicea, Sarsaparilla).
- What is the active ingredient?
- Potassium chloride, Prunus spinosa flower bud, Silicon dioxide, Smilax ornata root.
- Who is the labeler?
- Applied Bioenergetics, LLC, NDC labeler code 81425. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for LUMOe SKIN1 Skin Remedy?
- None: this is the only finished product listed under this name.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.