Real Relief NDC 71971-9204

NDC codes

FDA NDC Directory

Product NDC (as listed)71971-9204Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71971-9204Add 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
71971-9204-4	71971920404	30 mL in 1 BOTTLE (71971-9204-4)Marketed from Mar 3, 2018
71971-9204-5	71971920405	1 BOTTLE in 1 CARTON (71971-9204-5) / 100 mL in 1 BOTTLEMarketed from Mar 3, 2018
71971-9204-9	71971920409	1 BOTTLE in 1 CARTON (71971-9204-9) / 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): Real Relief
Generic name (nonproprietary): drosera, arnica montana, bryonia, cetraria islandica, coccus cacti, corallium rubrum, stannum metallicum, camomilla, coffea 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]/100mLCorallium rubrum whole — 3 [hp_C]/100mLTin — 3 [hp_C]/100mLChamomile — 4 [hp_C]/100mLArabica coffee bean — 4 [hp_C]/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
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 71971-9204_fe047742-2f8f-476b-a842-3378be6b60fdSPL ID fe047742-2f8f-476b-a842-3378be6b60fdSPL set ID fc6a509a-f4c0-47e7-8693-906ba6e03923UNII 75O014T1HG, O80TY208ZW, 56K0VVT47P, BJ7YPN79A1, LZB7TFX1LT, 22Z32PWR7R, 387GMG9FH5, FGL3685T2X, 3SW678MX72
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

N471971920404 followed by a unit qualifier and the quantity

Package 71971-9204-04. 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 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)