What is NDC 43689-0062?

43689-0062 is the product NDC for Magnilife DB Pain Relieving Foot, Apis mellifera 3 [hp_X]/g + 2 more ingredients cream, listed with the FDA by The Magni Group, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Magnilife DB Pain Relieving Foot (Apis mellifera, Leontopodium nivale subsp. Alpinum whole, Sulfur).

What is the active ingredient?

Apis mellifera, Leontopodium nivale subsp. Alpinum whole flowering, Sulfur.

The Magni Group, Inc., NDC labeler code 43689. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Magnilife DB Pain Relieving Foot?

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.

Magnilife DB Pain Relieving Foot NDC 43689-0062

NDC codes

FDA NDC Directory

Product NDC (as listed)43689-0062Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43689-0062Add 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
43689-0062-1	4368900620143689006201	113 g in 1 JAR (43689-0062-1)Marketed from Jun 29, 2026
43689-0062-2	4368900620243689006202	1 JAR in 1 BOTTLE, UNIT-DOSE (43689-0062-2) / 113 g in 1 JARMarketed from Jun 29, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Magnilife DB Pain Relieving Foot
Generic name (nonproprietary): apis mellifera, leontopodium nivale subsp. alpinum whole, sulfur
Active ingredients: Apis mellifera — 3 [hp_X]/gLeontopodium nivale subsp. Alpinum whole flowering — 6 [hp_X]/gSulfur — 1 [hp_X]/g
Dosage form: Cream
Route: Topical
Labeler: The Magni Group, Inc.NDC labeler code 43689
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 29, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 43689-0062_558fce1b-b7a9-b8c7-e063-6394a90aeab5SPL ID 558fce1b-b7a9-b8c7-e063-6394a90aeab5SPL set ID 2c54728e-80b0-4466-9b50-4a69878c9027UNII 7S82P3R43Z, 7R4LQP52DM, 70FD1KFU70
Pharmacologic class: Standardized Insect Venom Allergenic Extract

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

N443689006201 followed by a unit qualifier and the quantity

Package 43689-0062-01. 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 Jul 1, 2026.

Indications (excerpt from the label)

Uses Temporarily relieves foot pain

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43689-0062

What is NDC 43689-0062?: 43689-0062 is the product NDC for Magnilife DB Pain Relieving Foot, Apis mellifera 3 [hp_X]/g + 2 more ingredients cream, listed with the FDA by The Magni Group, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Magnilife DB Pain Relieving Foot (Apis mellifera, Leontopodium nivale subsp. Alpinum whole, Sulfur).
What is the active ingredient?: Apis mellifera, Leontopodium nivale subsp. Alpinum whole flowering, Sulfur.
Who is the labeler?: The Magni Group, Inc., NDC labeler code 43689. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Magnilife DB Pain Relieving Foot?: 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.