What is NDC 80661-007?

80661-007 is the product NDC for Bem Bio Antiperspirant forest trails, Magnesium hydroxide 10 g/100g; Magnesium carbonate hydroxide 10 g/100g aerosol, spray, listed with the FDA by Aeroflex Industria de Aerosol Ltda. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Bem Bio Antiperspirant forest trails (Magnesium Hydroxide,Magnesium Carbonate Hydroxide).

What is the active ingredient?

Magnesium hydroxide, Magnesium carbonate hydroxide.

Aeroflex Industria de Aerosol Ltda, NDC labeler code 80661. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Bem Bio Antiperspirant forest trails?

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.

Bem Bio Antiperspirant forest trails NDC 80661-007

NDC codes

FDA NDC Directory

Product NDC (as listed)80661-007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width80661-0007Add 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
80661-007-01	8066100070180661000701	102 g in 1 CAN (80661-007-01)Marketed from Jun 15, 2022

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): Bem Bio Antiperspirant forest trails
Generic name (nonproprietary): magnesium hydroxide,magnesium carbonate hydroxide
Active ingredients: Magnesium hydroxide — 10 g/100gMagnesium carbonate hydroxide — 10 g/100g
Dosage form: Aerosol, Spray
Route: Topical
Labeler: Aeroflex Industria de Aerosol LtdaNDC labeler code 80661
Product type: Over-the-counter drug
Marketing category: Unapproved drug (other)
Marketing start: Jun 15, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 80661-007_42744978-d69b-66eb-e063-6294a90a69efSPL ID 42744978-d69b-66eb-e063-6294a90a69efSPL set ID 412f6498-9534-4682-91fb-c8c99b559c1fUNII NBZ3QY004S, YQO029V1L4
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N480661000701 followed by a unit qualifier and the quantity

Package 80661-0007-01. 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, 2025.

Indications (excerpt from the label)

Uses Reduces underarm wetness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 80661-007

What is NDC 80661-007?: 80661-007 is the product NDC for Bem Bio Antiperspirant forest trails, Magnesium hydroxide 10 g/100g; Magnesium carbonate hydroxide 10 g/100g aerosol, spray, listed with the FDA by Aeroflex Industria de Aerosol Ltda. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Bem Bio Antiperspirant forest trails (Magnesium Hydroxide,Magnesium Carbonate Hydroxide).
What is the active ingredient?: Magnesium hydroxide, Magnesium carbonate hydroxide.
Who is the labeler?: Aeroflex Industria de Aerosol Ltda, NDC labeler code 80661. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Bem Bio Antiperspirant forest trails?: 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.