Bactoflam NDC 61657-0052

NDC codes

FDA NDC Directory

Product NDC (as listed)61657-0052Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61657-0052Add 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
61657-0052-1	61657005201	30 mL in 1 BOTTLE, DROPPER (61657-0052-1)Marketed from Jun 10, 2011

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): Bactoflam
Generic name (nonproprietary): echinacea,baptisia,apis mellifica ,ferrum phosphoricum ,
Active ingredients: Echinacea, Unspecified — 3 [hp_X]/30mLBaptisia tinctoria root — 3 [hp_X]/30mLApis mellifera — 12 [hp_X]/30mLFerrum phosphoricum — 12 [hp_X]/30mLAtropa belladonna — 12 [hp_X]/30mLToxicodendron pubescens leaf — 12 [hp_X]/30mLArsenic trioxide — 12 [hp_X]/30mL
Dosage form: Liquid
Route: Oral
Labeler: WHITE MANUFACTURING INC. DBA MICRO WEST
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jun 10, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 61657-0052_b9708571-5b91-4644-e053-2995a90a6a12SPL ID b9708571-5b91-4644-e053-2995a90a6a12SPL set ID 3bf75ef6-fc67-4edb-9ed3-204b6af021ddUNII 4N9P6CC1DX, 5EF0HWI5WU, 7S82P3R43Z, 91GQH8I5F7, WQZ3G9PF0H, 6IO182RP7A, S7V92P67HO
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. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461657005201 followed by a unit qualifier and the quantity

Package 61657-0052-01. 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 21, 2021.

Indications (excerpt from the label)

INDICATIONS FOR THE TEMPORARY RELIEF OF HEAT, REDNESS, SWELLING DUE TO INFLAMMATION

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)