NDC codes

FDA NDC Directory
Product NDC (as listed)50845-0092Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50845-0092Add 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 NDC11-digit (billing)PackageCopy
50845-0092-2508450092021 BOTTLE, SPRAY in 1 CARTON (50845-0092-2) / 30 mL in 1 BOTTLE, SPRAY (50845-0092-1)Marketed from Apr 7, 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)
Menopause
Generic name (nonproprietary)
agnus castus, angelica sinensis radix, apis mellifica, aralia quinquefolia, arnica montana, cimicifuga racemosa, galium aparine, glycyrrhiza glabra, oophorinum suis, sepia, thuja occidentalis, viscum album
Active ingredients
Chaste tree — 3 [hp_X]/mLAngelica sinensis root — 3 [hp_X]/mLApis mellifera — 6 [hp_X]/mLAmerican ginseng — 3 [hp_X]/mLArnica montana whole — 6 [hp_X]/mLBlack cohosh — 3 [hp_X]/mLGalium aparine whole — 3 [hp_X]/mLGlycyrrhiza glabra — 3 [hp_X]/mLSus scrofa ovary — 30 [hp_C]/mLSepia officinalis juice — 30 [hp_X]/mLThuja occidentalis leafy twig — 6 [hp_X]/mLViscum album fruiting top — 3 [hp_X]/mL
Dosage form
Liquid
Route
Oral
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)
Identifiers
Product ID 50845-0092_2f80d111-fe7c-419f-8bbb-ef7dfb1017d6SPL ID 2f80d111-fe7c-419f-8bbb-ef7dfb1017d6SPL set ID 3e17fa78-f5c2-47eb-9bb6-075ccffd01b6UNII 433OSF3U8A, B66F4574UG, 7S82P3R43Z, 8W75VCV53Q, O80TY208ZW, K73E24S6X9, Z4B6561488, 2788Z9758H, S7YTV04R8O, QDL83WN8C2, 1NT28V9397, BK9092J5MP
Pharmacologic class
Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Standardized Insect Venom 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

N450845009202 followed by a unit qualifier and the quantity

Package 50845-0092-02. 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 .

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve these symptoms associated with hormonal imbalance, which may accompany menopause: •mood swings •hot flashes •irritability •vaginal dryness •lack of sexual vitality ** **These statements are based upon traditional homeopathic practice. 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)

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