NDC codes

FDA NDC Directory
Product NDC (as listed)62106-0623Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62106-0623Add 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
62106-0623-0621060623006210606230030 mL in 1 BOTTLE, GLASS (62106-0623-0)Marketed from Dec 18, 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)
Hfe
Generic name (nonproprietary)
apis mellifica, belladonna, caulophyllum thalictroides, cimicifuga racemosa, dioscorea villosa, gelsemium sempervirens, helonias dioica, magnesia phosphorica, oryctolagus cuniculus (rabbit) adrenal gland, oryctolagus cuniculus (rabbit) ovary, oryctolagus cuniculus (rabbit) uterus, viburnum opulus
Active ingredients
Dioscorea villosa root — 4 [hp_X]/30mLOryctolagus cuniculus ovary — 10 [hp_X]/30mLApis mellifera — 5 [hp_X]/30mLAtropa belladonna — 4 [hp_X]/30mLBlack cohosh — 6 [hp_X]/30mLCaulophyllum thalictroides root — 4 [hp_X]/30mLChamaelirium luteum root — 4 [hp_X]/30mLOryctolagus cuniculus adrenal gland — 10 [hp_X]/30mLViburnum opulus bark — 2 [hp_X]/30mLGelsemium sempervirens root — 8 [hp_X]/30mLMagnesium phosphate, Dibasic trihydrate — 10 [hp_X]/30mLOryctolagus cuniculus uterus — 10 [hp_X]/30mL
Dosage form
Liquid
Route
Oral
Labeler
Seroyal USANDC labeler code 62106
Product type
Over-the-counter drug
Marketing category
Unapproved homeopathic
Marketing start
Listing expires
Other FDA classes
Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 62106-0623_c7c0766c-5fa4-95e0-e053-2995a90ac48fSPL ID c7c0766c-5fa4-95e0-e053-2995a90ac48fSPL set ID 7d508fdd-ba8b-07ec-e053-2991aa0a29efUNII IWY3IWX2G8, XA09528U2R, 7S82P3R43Z, WQZ3G9PF0H, K73E24S6X9, JTJ6HH6YEH, DQV54Y5H3U, QGY289M89Q, T1UG6H6805, 639KR60Q1Q, HF539G9L3Q, NQX84Z32G6UPC 0883196138708
Pharmacologic class
Calculi Dissolution Agent; Osmotic Laxative; 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

N462106062300 followed by a unit qualifier and the quantity

Package 62106-0623-00. 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)

Uses Helps promote and maintain general female reproductive health. Product 'Uses' are based on Homeopathic Materia Medica and have not been clinically tested. These 'Uses' have not been evaluated by the Food and Drug Administration. Directions To be taken 20 minutes away from food. Place drops directly under the tongue or into ¼ oz of water. Adults and adolescents (12 years and older): Take 10 drops two to three times daily or as recommended by your healthcare practitioner. Children (under 12 years): Take under the direction of your healthcare practitioner.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62106-0623

What is NDC 62106-0623?
62106-0623 is the product NDC for Hfe, Dioscorea villosa root 4 [hp_X]/30mL + 11 more ingredients liquid, listed with the FDA by Seroyal USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hfe (Apis mellifica, Belladonna, Caulophyllum thalictroides, Cimicifuga racemosa, Dioscorea villosa, Gelsemium sempervirens, Helonias dioica, Magnesia phosphorica, Oryctolagus cuniculus (Rabbit) Adrenal Gland, Oryctolagus cuniculus (Rabbit) Ovary, Oryctolagus cuniculus (Rabbit) Uterus, Viburnum opulus).
What is the active ingredient?
Dioscorea villosa root, Oryctolagus cuniculus ovary, Apis mellifera, Atropa belladonna, Black cohosh, Caulophyllum thalictroides root, Chamaelirium luteum root, Oryctolagus cuniculus adrenal gland, Viburnum opulus bark, Gelsemium sempervirens root, Magnesium phosphate, Dibasic trihydrate, Oryctolagus cuniculus uterus.
Who is the labeler?
Seroyal USA, NDC labeler code 62106. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hfe?
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.

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