What is NDC 58264-0370?

58264-0370 is the product NDC for G-7, Betula pubescens flower bud 1 [hp_X]/mL; Betula pendula leaf 1 [hp_X]/mL solution, listed with the FDA by DNA Labs, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

G-7 (BETULA PUBESCENS FLOWER BUD and BETULA PENDULA LEAF).

What is the active ingredient?

Betula pubescens flower bud, Betula pendula leaf.

DNA Labs, Inc., NDC labeler code 58264. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for G-7?

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.

G-7 NDC 58264-0370 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0370Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0370Add 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
58264-0370-2	58264037002	59.14 mL in 1 BOTTLE, GLASS (58264-0370-2)Marketed from Jan 1, 1990

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): G-7
Generic name (nonproprietary): betula pubescens flower bud and betula pendula leaf
Active ingredients: Betula pubescens flower bud — 1 [hp_X]/mLBetula pendula leaf — 1 [hp_X]/mL
Dosage form: Solution
Route: Sublingual
Labeler: DNA Labs, Inc.NDC labeler code 58264
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1990
Listing expires: Dec 31, 2026
Identifiers: Product ID 58264-0370_2b531912-67dc-6172-e063-6394a90a178fSPL ID 2b531912-67dc-6172-e063-6394a90a178fSPL set ID 4f45aef4-def2-4464-9a17-19db9cb64985UNII 32JS91VU1G, 5HW39H9KDH

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

NDC on a medical claim

N458264037002 followed by a unit qualifier and the quantity

Package 58264-0370-02. 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 Jan 9, 2025.

Indications (excerpt from the label)

INDICATIONS Painful joints, allergies, fatigue.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 58264-0370

What is NDC 58264-0370?: 58264-0370 is the product NDC for G-7, Betula pubescens flower bud 1 [hp_X]/mL; Betula pendula leaf 1 [hp_X]/mL solution, listed with the FDA by DNA Labs, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: G-7 (BETULA PUBESCENS FLOWER BUD and BETULA PENDULA LEAF).
What is the active ingredient?: Betula pubescens flower bud, Betula pendula leaf.
Who is the labeler?: DNA Labs, Inc., NDC labeler code 58264. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for G-7?: 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.