NDC codes

FDA NDC Directory
Product NDC (as listed)73716-001Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73716-0001Add 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 NDC11-digit (billing)PackageCopy
73716-001-10737160001101 g in 1 BLISTER PACK (73716-001-10)Marketed from Apr 17, 2020

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
BiopHresh
Generic name (nonproprietary)
kreosotum 6c, nitricum acidum 6c, thuja occidentalis 6c, pulsatilla vulgaris 6c, sepia officinalis 6c
Active ingredients
Thuja occidentalis leafy twig — 6 [hp_C]/gPulsatilla vulgaris — 6 [hp_C]/gSepia officinalis whole — 6 [hp_C]/gWood creosote — 6 [hp_C]/gNitric acid — 6 [hp_C]/g
Dosage form
Suppository
Route
Vaginal
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 73716-001_395f9684-88e0-bc34-e063-6394a90afdd8SPL ID 395f9684-88e0-bc34-e063-6394a90afdd8SPL set ID a3ae582a-edb1-3a46-e053-2995a90a901aUNII 1NT28V9397, I76KB35JEV, 48GD5780QF, 3JYG22FD73, 411VRN1TV4

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N473716000110 followed by a unit qualifier and the quantity

Package 73716-0001-10. 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 .

Indications (excerpt from the label)

Uses for the temporary relief of symptoms of bacterial vaginosis due to bacterial imbalance in the vagina including unusual vaginal odor, itching, irritaiton, or abnormal discharge. 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)

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