Kids Relief NDC 63388-915

NDC codes

FDA NDC Directory

Product NDC (as listed)63388-915Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63388-0915Add 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
63388-915-14	63388091514	30 mL in 1 BOTTLE (63388-915-14)Marketed from Mar 3, 2018
63388-915-15	63388091515	1 BOTTLE in 1 CARTON (63388-915-15) / 100 mL in 1 BOTTLEMarketed from Mar 3, 2018
63388-915-19	63388091519	1 BOTTLE in 1 CARTON (63388-915-19) / 250 mL in 1 BOTTLEMarketed from Mar 3, 2018

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): Kids Relief
Generic name (nonproprietary): drosera, arnica montana, bryonia, cetraria islandica, coccus cacti, corallium rubrum, stannum metallicum, chamomilla, coffee crudea
Active ingredients: Drosera rotundifolia flowering top — 1 [hp_C]/100mLArnica montana — 3 [hp_C]/100mLBryonia alba whole — 3 [hp_C]/100mLCetraria islandica subsp. Islandica — 1 [hp_C]/100mLProtortonia cacti — 3 [hp_C]/100mLTin — 3 [hp_C]/100mLChamomile — 4 [hp_C]/100mLArabica coffee bean — 4 [hp_C]/100mLCorallium rubrum whole — 3 [hp_C]/100mL
Dosage form: Liquid
Route: Oral
Labeler: Laboratoire Atlas Inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 63388-915_40aacaf1-ccd0-3ffb-e063-6394a90aa4dfSPL ID 40aacaf1-ccd0-3ffb-e063-6394a90aa4dfSPL set ID de020891-eca2-405c-81cd-75dfb4ffe586UNII 75O014T1HG, O80TY208ZW, 56K0VVT47P, BJ7YPN79A1, LZB7TFX1LT, 387GMG9FH5, FGL3685T2X, 3SW678MX72, 22Z32PWR7R
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

N463388091514 followed by a unit qualifier and the quantity

Package 63388-0915-14. 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 Oct 8, 2025.

Indications (excerpt from the label)

Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve symptoms associated with nighttime cough and cold: •dry cough •cough with expectoration •chest congestion •fever •aches and pains

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)