Sleepy Time CP NDC 43406-0675

NDC codes

FDA NDC Directory

Product NDC (as listed)43406-0675Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43406-0675Add 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
43406-0675-1	43406067501	30 mL in 1 BOTTLE, DROPPER (43406-0675-1)Marketed from Apr 30, 2018

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): Sleepy Time CP
Generic name (nonproprietary): aconitum, arsenicum alb, calc carb, coffea cruda, magnesium met, nux vom, pulsatilla, sepia, sulphur
Active ingredients: Aconitum napellus whole — 30 [hp_X]/mLArsenic trioxide — 30 [hp_X]/mLOyster shell calcium carbonate, Crude — 30 [hp_X]/mLArabica coffee bean — 30 [hp_X]/mLMagnesium — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLSulfur — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Natural Creations, Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Apr 30, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 43406-0675_b30c6c13-693d-4b4a-b6f6-e1a0f196c1c4SPL ID b30c6c13-693d-4b4a-b6f6-e1a0f196c1c4SPL set ID 03cbb408-7e2a-49e8-b83a-b8d932a10459UNII U0NQ8555JD, S7V92P67HO, 2E32821G6I, 3SW678MX72, I38ZP9992A, 269XH13919, I76KB35JEV, QDL83WN8C2, 70FD1KFU70UPC 0877730002716
Pharmacologic class: Non-Standardized Food Allergenic Extract; Non-Standardized Plant 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

N443406067501 followed by a unit qualifier and the quantity

Package 43406-0675-01. 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 Dec 16, 2025.

Indications (excerpt from the label)

USES: Temporarily relieves occasional sleeplessness.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)