What is NDC 81488-003?

81488-003 is the product NDC for Mineffect facial skin protectant and acne treatment solution, Aluminum oxide 7 [hp_X]/118mL + 7 more ingredients spray, listed with the FDA by Kadesh Incoporation Co,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Mineffect facial skin protectant and acne treatment solution (Alumina, Calcarea Silicata, Ferrum Metallicum, Magnesia Sulphurica, Phosphorus, Sulphur, Titanium Metallicum, Zincum Metallicum).

What is the active ingredient?

Aluminum oxide, Calcium silicate, Iron, Magnesium sulfate heptahydrate, Phosphorus, Sulfur, Titanium, Zinc.

Kadesh Incoporation Co,Ltd, NDC labeler code 81488. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mineffect facial skin protectant and acne treatment solution?

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.

NDC 81488-003

NDC codes

FDA NDC Directory

Product NDC (as listed)81488-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width81488-0003Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
81488-003-04	8148800030481488000304	1 BOTTLE, SPRAY in 1 BOX (81488-003-04) / 118 mL in 1 BOTTLE, SPRAYMarketed from Feb 1, 2021

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): Mineffect facial skin protectant and acne treatment solution
Generic name (nonproprietary): alumina, calcarea silicata, ferrum metallicum, magnesia sulphurica, phosphorus, sulphur, titanium metallicum, zincum metallicum
Active ingredients: Aluminum oxide — 7 [hp_X]/118mLCalcium silicate — 5 [hp_X]/118mLIron — 7 [hp_X]/118mLMagnesium sulfate heptahydrate — 7 [hp_X]/118mLPhosphorus — 6 [hp_X]/118mLSulfur — 4 [hp_X]/118mLTitanium — 7 [hp_X]/118mLZinc — 8 [hp_X]/118mL
Dosage form: Spray
Route: Topical
Labeler: Kadesh Incoporation Co,LtdNDC labeler code 81488
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 81488-003_0906a66d-7248-a993-e063-6394a90a7150SPL ID 0906a66d-7248-a993-e063-6394a90a7150SPL set ID f6b3ea92-2382-4c3f-8ed9-31ea26fd47eeUNII LMI26O6933, S4255P4G5M, E1UOL152H7, SK47B8698T, 27YLU75U4W, 70FD1KFU70, D1JT611TNE, J41CSQ7QDS
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Osmotic Laxative; Phosphate Binder

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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N481488000304 followed by a unit qualifier and the quantity

Package 81488-0003-04. 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 Oct 31, 2023.

Indications (excerpt from the label)

Uses • For the treatment of acne • Helps keep skin clear of new acne blemishes, acne pimples and breakouts. • Temporarily protects and helps to relieve minor skin irritation and itching due to *rashes *eczema.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 81488-003

What is NDC 81488-003?: 81488-003 is the product NDC for Mineffect facial skin protectant and acne treatment solution, Aluminum oxide 7 [hp_X]/118mL + 7 more ingredients spray, listed with the FDA by Kadesh Incoporation Co,Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mineffect facial skin protectant and acne treatment solution (Alumina, Calcarea Silicata, Ferrum Metallicum, Magnesia Sulphurica, Phosphorus, Sulphur, Titanium Metallicum, Zincum Metallicum).
What is the active ingredient?: Aluminum oxide, Calcium silicate, Iron, Magnesium sulfate heptahydrate, Phosphorus, Sulfur, Titanium, Zinc.
Who is the labeler?: Kadesh Incoporation Co,Ltd, NDC labeler code 81488. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mineffect facial skin protectant and acne treatment solution?: 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.

Mineffect facial skin protectant and acne treatment solution NDC 81488-003