Childrens Cold and Cough Nighttime NDC 0363-9996

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-9996Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-9996Add 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
0363-9996-01	00363999601	118 mL in 1 BOTTLE, PLASTIC (0363-9996-01)Marketed from Feb 1, 2019

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Childrens Cold and Cough Nighttime
Generic name (nonproprietary): onion, calcium sulfide, sodium chloride, anemone pulsatilla, arabica coffee bean, matricaria chamomilla, sulfur, phosphorus and goldenseal
Active ingredients: Sodium chloride — 6 [hp_X]/mLAnemone pulsatilla — 6 [hp_X]/mLMatricaria chamomilla — 6 [hp_X]/mLGoldenseal — 6 [hp_X]/mLArabica coffee bean — 6 [hp_X]/mLSulfur — 12 [hp_X]/mLPhosphorus — 12 [hp_X]/mLOnion — 6 [hp_X]/mLCalcium sulfide — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Walgreen Company
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 1, 2019
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)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 0363-9996_efe0ec6b-9901-858f-e053-2a95a90aec59SPL ID efe0ec6b-9901-858f-e053-2a95a90aec59SPL set ID 80c41b65-0411-4395-e053-2a91aa0a9df9UNII 451W47IQ8X, I76KB35JEV, G0R4UBI2ZZ, ZW3Z11D0JV, 3SW678MX72, 70FD1KFU70, 27YLU75U4W, 492225Q21H, 1MBW07J51Q
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

N400363999601 followed by a unit qualifier and the quantity

Package 00363-9996-01. 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 15, 2022.

Indications (excerpt from the label)

Uses Temporarily relieves the symptoms of the common cold including cough, runny nose, sneezing, nasal or chest congestion or sore throat with accompanying occasional sleeplessness.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)