NDC codes

FDA NDC Directory
Product NDC (as listed)83027-0152Labeler and product segments. Claims need a package NDC.
Product NDC at billing width83027-0152Add 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
83027-0152-18302701520160 mL in 1 BOTTLE, SPRAY (83027-0152-1)Marketed from Apr 29, 2025

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)
Bacti Sode
Generic name (nonproprietary)
bacillus tetani, chlamydia trachomatis, colibacillinum cum natrum muriaticum, klebsiella pneumoniae, mycobacterium paratuberculosis, mycoplasma pneumoniae, pneumococcinum, salmonella typhi nosode, staphylococcus aureus, streptococcus viridans, pyrogenium, pertussinum, streptococcus agalactiae, streptococcus dysgalactiae, streptococcus mutans, bacillus cereus
Active ingredients
Clostridium tetani — 20 [hp_X]/mLChlamydia trachomatis — 20 [hp_X]/mLEscherichia coli — 20 [hp_X]/mLKlebsiella pneumoniae — 20 [hp_X]/mLMycobacterium avium subsp. Paratuberculosis — 20 [hp_X]/mLMycoplasma pneumoniae — 20 [hp_X]/mLStreptococcus pneumoniae — 20 [hp_X]/mLSalmonella enterica enterica serovar typhi — 20 [hp_X]/mLStaphylococcus aureus — 20 [hp_X]/mLStreptococcus viridans group — 20 [hp_X]/mLRancid beef — 20 [hp_X]/mLHuman sputum, Bordetella pertussis infected — 30 [hp_X]/mLStreptococcus agalactiae — 15 [hp_C]/mLStreptococcus dysgalactiae — 15 [hp_C]/mLStreptococcus mutans — 15 [hp_C]/mLBacillus cereus — 18 [hp_C]/mL
Dosage form
Spray
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Identifiers
Product ID 83027-0152_3a8f0bb4-9f0d-4cb8-b343-3cf2d1ba1391SPL ID 3a8f0bb4-9f0d-4cb8-b343-3cf2d1ba1391SPL set ID 5a56ddc9-2550-4a6a-a553-3bc919b844f0UNII 751E8J54VM, T6NI39QU44, 514B9K0L10, 09PA36CT5R, XH0F4IP2RX, JQE470FAD0, BT6U234YR2, 760T5R8B3O, O478WX4004, NNV2379HKR, 29SUH5R3HU, U364V64HUN, 2B3763S671, LN0SH02Y5M, 5C7J33MJJ1, 7YC151N82LUPC 0649818014023

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

N483027015201 followed by a unit qualifier and the quantity

Package 83027-0152-01. 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 .

Indications (excerpt from the label)

USES: Aids in temporary relief of •headache, •runny nose, •sweats, chills, minor cough, fatigue, and mild abdominal discomfort.† †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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