Sleep HP NDC 70163-0002

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0002Add 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
70163-0002-1	70163000201	30 mL in 1 BOTTLE, DROPPER (70163-0002-1)Marketed from Nov 30, 2020

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): Sleep HP
Generic name (nonproprietary): arsenicum album, avena sativa, coffea cruda, kali carbonicum, magnesia carbonica, nux vomica, passiflora incarnata, sepia, valeriana officinalis
Active ingredients: Arsenic trioxide — 30 [hp_X]/mLAvena sativa flowering top — 30 [hp_X]/mLArabica coffee bean — 30 [hp_X]/mLPotassium carbonate — 30 1/mLMagnesium carbonate — 30 [hp_X]/mLStrychnos nux-vomica seed — 30 [hp_X]/mLPassiflora incarnata flowering top — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLValerian — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Grato Holdings, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 30, 2020
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 70163-0002_f934b0f4-d90e-42ff-9226-839dd03bcb38SPL ID f934b0f4-d90e-42ff-9226-839dd03bcb38SPL set ID 90e8553a-cfa9-4bb1-a398-3242a4e7456bUNII S7V92P67HO, MA9CQJ3F7F, 3SW678MX72, BQN1B9B9HA, 0E53J927NA, 269XH13919, CLF5YFS11O, QDL83WN8C2, JWF5YAW3QWUPC 0363113700954
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

N470163000201 followed by a unit qualifier and the quantity

Package 70163-0002-01. 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 Nov 30, 2020.

Indications (excerpt from the label)

INDICATIONS: May temporary relieve symptoms due to fatigue and restlessness from inability to sleep.** **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)