What is NDC 50845-0274?

50845-0274 is the product NDC for Fem Flora Defense, Baptisia tinctoria root 3 [hp_X]/mL + 11 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Fem Flora Defense (Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (Angustifolia), Nitricum Acidum, Pulsatilla (Pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis).

What is the active ingredient?

Baptisia tinctoria root, Sodium borate, Candida albicans, Candida parapsilosis, Cinchona officinalis bark, Echinacea angustifolia whole, Nitric acid, Pulsatilla pratensis whole, Rancid beef, Sepia officinalis juice, Sulfuric acid, Thuja occidentalis leafy twig.

Liddell Laboratories, Inc., NDC labeler code 50845. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Fem Flora Defense?

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.

Fem Flora Defense NDC 50845-0274 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)50845-0274Labeler and product segments. Claims need a package NDC.

Product NDC at billing width50845-0274Add 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
50845-0274-1	5084502740150845027401	30 mL in 1 BOTTLE, SPRAY (50845-0274-1)Marketed from Apr 22, 2021

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): Fem Flora Defense
Generic name (nonproprietary): baptisia tinctoria, borax, candida albicans, candida parapsilosis, cinchona officinalis, echinacea (angustifolia), nitricum acidum, pulsatilla (pratensis), pyrogenium, sepia, sulphuricum acidum, thuja occidentalis
Active ingredients: Baptisia tinctoria root — 3 [hp_X]/mLSodium borate — 30 [hp_C]/mLCandida albicans — 12 [hp_X]/mLCandida parapsilosis — 8 [hp_C]/mLCinchona officinalis bark — 30 [hp_C]/mLEchinacea angustifolia whole — 3 [hp_X]/mLNitric acid — 30 [hp_C]/mLPulsatilla pratensis whole — 30 [hp_C]/mLRancid beef — 200 [hp_C]/mLSepia officinalis juice — 30 [hp_C]/mLSulfuric acid — 30 [hp_C]/mLThuja occidentalis leafy twig — 30 [hp_C]/mL
Dosage form: Spray
Route: Oral
Labeler: Liddell Laboratories, Inc.NDC labeler code 50845
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 22, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Fungal Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)
Identifiers: Product ID 50845-0274_6a28ccf7-80a2-4db1-a1aa-ec417335b8aeSPL ID 6a28ccf7-80a2-4db1-a1aa-ec417335b8aeSPL set ID 8015e1cb-9ebd-4b3e-af57-92f2754fb790UNII 5EF0HWI5WU, 91MBZ8H3QO, 4D7G21HDBC, 0KZ676D44N, S003A158SB, VB06AV5US8, 411VRN1TV4, 8E272251DI, 29SUH5R3HU, QDL83WN8C2, O40UQP6WCF, 1NT28V9397UPC 0363113117967
Pharmacologic class: Non-Standardized Fungal 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

N450845027401 followed by a unit qualifier and the quantity

Package 50845-0274-01. 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 Aug 17, 2023.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.** **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50845-0274

What is NDC 50845-0274?: 50845-0274 is the product NDC for Fem Flora Defense, Baptisia tinctoria root 3 [hp_X]/mL + 11 more ingredients spray, listed with the FDA by Liddell Laboratories, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fem Flora Defense (Baptisia Tinctoria, Borax, Candida Albicans, Candida Parapsilosis, Cinchona Officinalis, Echinacea (Angustifolia), Nitricum Acidum, Pulsatilla (Pratensis), Pyrogenium, Sepia, Sulphuricum Acidum, Thuja Occidentalis).
What is the active ingredient?: Baptisia tinctoria root, Sodium borate, Candida albicans, Candida parapsilosis, Cinchona officinalis bark, Echinacea angustifolia whole, Nitric acid, Pulsatilla pratensis whole, Rancid beef, Sepia officinalis juice, Sulfuric acid, Thuja occidentalis leafy twig.
Who is the labeler?: Liddell Laboratories, Inc., NDC labeler code 50845. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Fem Flora Defense?: 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.