What is NDC 71971-9060?

71971-9060 is the product NDC for Kids Relief Teething Oral Liquid, Matricaria recutita 5 [hp_C]/25mL + 3 more ingredients liquid, listed with the FDA by Homeolab International (Canada) inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Kids Relief Teething Oral Liquid (Chamomilla, arnica montana, borax, hypericum perforatum liquid).

What is the active ingredient?

Matricaria recutita, Arnica montana, Sodium borate, Hypericum perforatum.

Homeolab International (Canada) inc, NDC labeler code 71971. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Kids Relief Teething Oral Liquid?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Kids Relief Teething Oral Liquid NDC 71971-9060

NDC codes

FDA NDC Directory

Product NDC (as listed)71971-9060Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71971-9060Add 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
71971-9060-8	7197190600871971906008	1 BOTTLE in 1 CARTON (71971-9060-8) / 25 mL in 1 BOTTLEMarketed from Mar 3, 2017

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 Teething Oral LiquidSuffix: Teething Oral Liquid
Generic name (nonproprietary): chamomilla, arnica montana, borax, hypericum perforatum liquid
Active ingredients: Matricaria recutita — 5 [hp_C]/25mLArnica montana — 5 [hp_C]/25mLSodium borate — 5 [hp_C]/25mLHypericum perforatum — 5 [hp_C]/25mL
Dosage form: Liquid
Route: Oral
Labeler: Homeolab International (Canada) incNDC labeler code 71971
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 3, 2017
Listing expires: Dec 31, 2026
Identifiers: Product ID 71971-9060_cb5c8a1b-fa0f-4f18-bc34-028c9d46401fSPL ID cb5c8a1b-fa0f-4f18-bc34-028c9d46401fSPL set ID df6edd7a-3ca6-4946-b083-1193f4b1d226UNII G0R4UBI2ZZ, O80TY208ZW, 91MBZ8H3QO, XK4IUX8MNB

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

N471971906008 followed by a unit qualifier and the quantity

Package 71971-9060-08. 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 Jul 16, 2019.

Indications (excerpt from the label)

Uses This homeopathic medicine is made from a combination of ingredients traditionally used to help relieve indispositions caused by teething*: • gum inflammation • gum pain • fever • diarrhea • restlessness and irritability

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71971-9060

What is NDC 71971-9060?: 71971-9060 is the product NDC for Kids Relief Teething Oral Liquid, Matricaria recutita 5 [hp_C]/25mL + 3 more ingredients liquid, listed with the FDA by Homeolab International (Canada) inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Kids Relief Teething Oral Liquid (Chamomilla, arnica montana, borax, hypericum perforatum liquid).
What is the active ingredient?: Matricaria recutita, Arnica montana, Sodium borate, Hypericum perforatum.
Who is the labeler?: Homeolab International (Canada) inc, NDC labeler code 71971. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Kids Relief Teething Oral Liquid?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.