RET Bladder 7006 (ret bladder) NDC 63083-7006

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7006Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7006Add 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
63083-7006-1	63083700601	29.5 mL in 1 BOTTLE, DROPPER (63083-7006-1)Marketed from Aug 15, 1985

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): RET Bladder 7006Suffix: 7006
Generic name (nonproprietary): ret bladder
Active ingredients: Centaurium erythraea flowering top — 3 [hp_X]/29.5mLCeratostigma willmottianum flowering top — 3 [hp_X]/29.5mLCarpinus betulus flower — 3 [hp_X]/29.5mLSalix alba flowering top — 3 [hp_X]/29.5mLPotassium phosphate, Unspecified form — 3 [hp_X]/29.5mLSodium chloride — 3 [hp_X]/29.5mLPotassium alum — 30 [hp_X]/29.5mLApis mellifera — 30 [hp_X]/29.5mLActivated charcoal — 30 [hp_X]/29.5mLArtemisia cina pre-flowering top — 30 [hp_X]/29.5mLPulsatilla montana whole — 30 [hp_X]/29.5mLSepia officinalis juice — 30 [hp_X]/29.5mLSpongia officinalis skeleton, Roasted — 30 [hp_X]/29.5mLDelphinium staphisagria seed — 30 [hp_X]/29.5mLVeratrum album root — 30 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health Formulas
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 15, 1984
Listing expires: Dec 31, 2027
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)
Identifiers: Product ID 63083-7006_6164ed7f-5c4f-4ad1-b445-a3556655e4aeSPL ID 6164ed7f-5c4f-4ad1-b445-a3556655e4aeSPL set ID f1d354e7-3d72-40aa-aaf1-172cb39f0711UNII ZL25KMM82T, S13FA2GQG9, 07YL55QKZ9, XBP5X7E70R, B7862WZ632, 451W47IQ8X, 1L24V9R23S, 7S82P3R43Z, 2P3VWU3H10, 28M1820ACT, 24K790T39B, QDL83WN8C2, 1PIP394IID, 00543AP1JV, QNS6W5US1Z
Pharmacologic class: 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

N463083700601 followed by a unit qualifier and the quantity

Package 63083-7006-01. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS Temporarily relieves passiveness or being weak-willed, lacking confidence or trust in ones self, mental weariness, staleness in life, self-pity, bitterness, grief, despair, or sadness.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)