Kids Relief NDC 71971-9104

NDC codes

FDA NDC Directory

Product NDC (as listed)71971-9104Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71971-9104Add 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
71971-9104-4	71971910404	30 mL in 1 BOTTLE (71971-9104-4)Marketed from Mar 3, 2018
71971-9104-5	71971910405	1 BOTTLE in 1 CARTON (71971-9104-5) / 100 mL in 1 BOTTLEMarketed from Mar 3, 2018
71971-9104-9	71971910409	1 BOTTLE in 1 CARTON (71971-9104-9) / 250 mL in 1 BOTTLEMarketed from Mar 3, 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): Kids Relief
Generic name (nonproprietary): asafoetida, ignatia amara, valeriana officinalis, avena sativa, argentum nitricum, hyoscyamus niger, paeonia officinalis, stramonium, cocculus indicus
Active ingredients: Asafetida — 8 [hp_X]/100mLStrychnos ignatii seed — 8 [hp_X]/100mLValeriana officinalis whole — 8 [hp_X]/100mLOat bran — 8 [hp_X]/100mLSilver nitrate — 8 [hp_X]/100mLHyoscyamus niger — 8 [hp_X]/100mLPaeonia officinalis root — 8 [hp_X]/100mLDatura stramonium — 8 [hp_X]/100mLAnamirta cocculus whole — 8 [hp_X]/100mL
Dosage form: Liquid
Route: Oral
Labeler: Homeolab International (Canada) inc
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 71971-9104_93a1a99e-bfd0-4818-92b9-b64f2c775f05SPL ID 93a1a99e-bfd0-4818-92b9-b64f2c775f05SPL set ID ce7273d4-01f8-4b6b-b33a-83bd2d4fb07aUNII W9FZA51AS1, 1NM3M2487K, FP6O7F1X9R, KQX236OK4U, 95IT3W8JZE, 4WRK2153H3, 8R564U2E1P, G6W4F0V8Z3, 8O4P2U3QO2

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

N471971910404 followed by a unit qualifier and the quantity

Package 71971-9104-04. 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 10, 2019.

Indications (excerpt from the label)

•Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve symptoms of: •Restlessness •nervousness •irritability •agitation •sleeplessness lessens nightmares

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)