NDC codes

FDA NDC Directory
Product NDC (as listed)84999-007Labeler and product segments. Claims need a package NDC.
Product NDC at billing width84999-0007Add 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
84999-007-01849990007011 BOTTLE, SPRAY in 1 CARTON (84999-007-01) / 30 mL in 1 BOTTLE, SPRAYMarketed from Feb 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

Generic name (nonproprietary)
kali sulphuricum
Active ingredients
Potassium sulfate — 6 [hp_X]/30mL
Dosage form
Spray
Route
Oral
Labeler
Martin & Pleasance Pty LtdNDC labeler code 84999
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers
Product ID 84999-007_395844ca-6baa-db3e-e063-6294a90a7726SPL ID 395844ca-6baa-db3e-e063-6294a90a7726SPL set ID 0fa37814-6c70-4834-a0dc-5e729b80f3e5UNII 1K573LC5TV
Pharmacologic class
Osmotic Laxative; 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

N484999000701 followed by a unit qualifier and the quantity

Package 84999-0007-01. 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: Dry, scaly skin Minor skin eruptions Dandru­ff

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 84999-007

What is NDC 84999-007?
84999-007 is the product NDC for Schuessler Tissue Salts Kali Sulph Skin Balance 7, Potassium sulfate 6 [hp_X]/30mL spray, listed with the FDA by Martin & Pleasance Pty Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Schuessler Tissue Salts Kali Sulph Skin Balance 7 (Kali Sulphuricum).
What is the active ingredient?
Potassium sulfate.
Who is the labeler?
Martin & Pleasance Pty Ltd, NDC labeler code 84999. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Schuessler Tissue Salts Kali Sulph Skin Balance 7?
1 other product NDC are listed under this name. See all Schuessler Tissue Salts Kali Sulph Skin Balance 7 NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Schuessler Tissue Salts Kali Sulph Skin Balance 7 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Schuessler Tissue Salts Kali Sulph Skin Balance 7kali sulphuricumPotassium sulfate 6 [hp_X]/1Tablet, ChewableOralMartin & Pleasance Pty Ltd84999-01984999-0019-01

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