NDC codes

FDA NDC Directory
Product NDC (as listed)84999-030Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84999-0030Add 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
84999-030-01849990030011 BOTTLE, SPRAY in 1 CARTON (84999-030-01) / 30 mL in 1 BOTTLE, SPRAYMarketed from Aug 1, 2025

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)
Schuessler Tissue Salts Comb 12 General Tonic
Generic name (nonproprietary)
calcarea fluorica,calcarea phosphorica,calcarea sulphurica,ferrum phosphoricum ,kali phosphoricum,kali muriaticum,kali sulphuricum,magnesia phosphorica,natrum muriaticum,natrum phosphoricum,natrum sulphuricum,silicea
Active ingredients
Calcium fluoride — 6 [hp_X]/30mLTribasic calcium phosphate — 6 [hp_X]/30mLCalcium sulfate dihydrate — 6 [hp_X]/30mLFerrous phosphate — 6 [hp_X]/30mLDibasic potassium phosphate — 6 [hp_X]/30mLPotassium chloride — 6 [hp_X]/30mLMagnesium phosphate, Dibasic — 6 [hp_X]/30mLPotassium sulfate — 6 [hp_X]/30mLSodium chloride — 6 [hp_X]/30mLSodium phosphate, Dibasic, Anhydrous — 6 [hp_X]/30mLSodium sulfate anhydrous — 6 [hp_X]/30mLSilicon dioxide — 6 [hp_X]/30mL
Dosage form
Spray
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Phosphate Chelating Activity (Mechanism)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers
Product ID 84999-030_3e49a812-789c-646c-e063-6294a90a5830SPL ID 3e49a812-789c-646c-e063-6294a90a5830SPL set ID c14c79ab-85bb-45f2-83d1-1d9c298ffdfdUNII O3B55K4YKI, 91D9GV0Z28, 4846Q921YM, D07L04MRWI, CI71S98N1Z, 660YQ98I10, A1Y870209Z, 1K573LC5TV, 451W47IQ8X, 22ADO53M6F, 36KCS0R750, ETJ7Z6XBU4
Pharmacologic class
Blood Coagulation Factor; Osmotic Laxative; Phosphate Binder; Potassium Salt

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

N484999003001 followed by a unit qualifier and the quantity

Package 84999-0030-01. 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 Temporarily relieves symptoms associated with: General debility Fatigue Exhaustion Tension

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

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