Grief NDC 43742-1513

NDC codes

FDA NDC Directory

Product NDC (as listed)43742-1513Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43742-1513Add 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
43742-1513-1	43742151301	30 mL in 1 BOTTLE, DROPPER (43742-1513-1)Marketed from Jul 26, 2019

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): Grief
Generic name (nonproprietary): cimicifuga racemosa, natrum sulphuricum, phosphoricum acidum, sepia, cerebrum suis, ignatia amara, natrum muriaticum, ambra grisea, dna, aurum metallicum, cocculus indicus, digitalis purpurea, helleborus niger, lycopodium clavatum, staphysagria
Active ingredients: Black cohosh — 6 [hp_X]/mLSodium sulfate — 6 [hp_X]/mLPhosphoric acid — 6 [hp_X]/mLSepia officinalis juice — 8 [hp_X]/mLSus scrofa cerebrum — 8 [hp_X]/mLStrychnos ignatii seed — 8 [hp_X]/mLSodium chloride — 8 [hp_X]/mLAmbergris — 9 [hp_X]/mLHerring sperm DNA — 10 [hp_X]/mLGold — 12 [hp_X]/mLAnamirta cocculus seed — 12 [hp_X]/mLDigitalis — 12 [hp_X]/mLHelleborus niger root — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLDelphinium staphisagria seed — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Deseret Biologicals, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 26, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 43742-1513_e61360cc-da3b-4d07-962f-3d6d903d892aSPL ID e61360cc-da3b-4d07-962f-3d6d903d892aSPL set ID e7ff1297-512e-4e95-a918-1c57fa3a50ddUNII K73E24S6X9, 0YPR65R21J, E4GA8884NN, QDL83WN8C2, 4GB5DQR532, 1NM3M2487K, 451W47IQ8X, XTC0D02P6C, 51FI676N6F, 79Y1949PYO, 810258W28U, F1T8QT9U8B, 608DGJ6815, C88X29Y479, 00543AP1JVUPC 0810151883748
Pharmacologic class: Standardized Chemical Allergen

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

N443742151301 followed by a unit qualifier and the quantity

Package 43742-1513-01. 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 Mar 25, 2024.

Indications (excerpt from the label)

USES: • For the temporary relief of symptoms including: • grief • shock • denial • weeping • forsakenness • lack of emotion • sighing These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)