D-53 NDC 58264-0053

NDC codes

FDA NDC Directory

Product NDC (as listed)58264-0053Labeler and product segments. Claims need a package NDC.

Product NDC at billing width58264-0053Add 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
58264-0053-1	58264005301	29.57 mL in 1 BOTTLE, GLASS (58264-0053-1)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): D-53
Generic name (nonproprietary): ammonium bromide, bromine, calcium sulfide, potassium bromide, rhododendron tomentosum leafy twig, sodium bromide, sodium chloride, and bos taurus placenta
Active ingredients: Ammonium bromide — 12 [hp_X]/mLBromine — 12 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mLPotassium bromide — 12 [hp_X]/mLRhododendron tomentosum leafy twig — 12 [hp_X]/mLSodium bromide — 12 [hp_X]/mLSodium chloride — 30 [hp_X]/mLBos taurus placenta — 12 [hp_X]/mL
Dosage form: Solution
Route: Sublingual
Labeler: DNA Labs, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 1990
Listing expires: Dec 31, 2026
Identifiers: Product ID 58264-0053_2b9ec8dd-73b0-e366-e063-6394a90ae792SPL ID 2b9ec8dd-73b0-e366-e063-6394a90ae792SPL set ID 3787d569-ee4d-41de-9519-73c11b626b38UNII R0JB3224WS, SBV4XY874G, 1MBW07J51Q, OSD78555ZM, 877L01IZ0P, LC1V549NOM, 451W47IQ8X, 83AL37E3A7

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

N458264005301 followed by a unit qualifier and the quantity

Package 58264-0053-01. 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 Jan 13, 2025.

Indications (excerpt from the label)

INDICATIONS Acne, pimples, rashes.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)