Para Solve NDC 61626-0107

NDC codes

FDA NDC Directory

Product NDC (as listed)61626-0107Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61626-0107Add 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
61626-0107-4	61626010704	59 mL in 1 BOTTLE (61626-0107-4)Marketed from Dec 4, 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): Para Solve
Generic name (nonproprietary): calc carb, chenopodium anth, cina, croton, filix mas, gambocia, granatum, lycopodium, merc corros, nat phos, santoninum, senna, spigelia anth, stannum met, tanacetum, teuricum mar, zingiber
Active ingredients: Oyster shell calcium carbonate, Crude — 12 [hp_X]/59.1mLDysphania ambrosioides — 12 [hp_X]/59.1mLArtemisia cina pre-flowering top — 12 [hp_X]/59.1mLCroton tiglium seed — 12 [hp_X]/59.1mLDryopteris filix-mas root — 12 [hp_X]/59.1mLGamboge — 12 [hp_X]/59.1mLPunica granatum root bark — 12 [hp_X]/59.1mLLycopodium clavatum spore — 12 [hp_X]/59.1mLMercuric chloride — 12 [hp_X]/59.1mLSodium phosphate, Dibasic, Heptahydrate — 12 [hp_X]/59.1mLSantonin — 12 [hp_X]/59.1mLSenna leaf — 12 [hp_X]/59.1mLSpigelia anthelmia — 12 [hp_X]/59.1mLTin — 12 [hp_X]/59.1mLTanacetum vulgare top — 12 [hp_X]/59.1mLTeucrium marum — 12 [hp_X]/59.1mLGinger — 12 [hp_X]/59.1mL
Dosage form: Liquid
Route: Oral
Labeler: NET Remedies
Product type: Prescription drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 4, 2018
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Histamine Release (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers: Product ID 61626-0107_b9492b5a-908a-4f3c-e053-2a95a90a6650SPL ID b9492b5a-908a-4f3c-e053-2a95a90a6650SPL set ID a58f6134-67f0-4691-8e9e-a93f48669d6aUNII 2E32821G6I, 4H5RSU087I, 28M1820ACT, 0HK2GZK66E, C0ZK0RRF5X, 7556HJ7587, CLV24I3T1D, C88X29Y479, 53GH7MZT1R, 70WT22SF4B, 1VL8J38ERO, AK7JF626KX, WYT05213GE, 387GMG9FH5, D52957JQ8M, 10464S0TAA, C5529G5JPQ
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

N461626010704 followed by a unit qualifier and the quantity

Package 61626-0107-04. 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 Jan 19, 2021.

Indications (excerpt from the label)

INDICATIONS FOR USE : For the temporary relief of gastrointestinal symptoms such as gas, bloating, stomach upset, abdominal discomfort which may be accompanied by pale face or circles under the eyes, bad breath, bariable appetite, localized ithching, postnasal drip, canker sores. irritability, back pain, resltess sleep, and sensitivity in lower right abdominal area. Temporary relief of cough.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)