What is NDC 63083-7011?

63083-7011 is the product NDC for RET Thyroid/Adrenal 7011 (ret thyroid/adrenal), Populus tremula flowering top 3 [hp_X]/29.5mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

RET Thyroid/Adrenal 7011 (RET Thyroid/Adrenal).

What is the active ingredient?

Populus tremula flowering top, Scleranthus annuus flowering top, Calcium sulfate anhydrous, Magnesium phosphate, Dibasic trihydrate, Silicon dioxide, Strychnos ignatii seed, Iodine, Lycopodium clavatum spore, Nutmeg, Smilax ornata root, Zinc.

Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for RET Thyroid/Adrenal 7011?

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.

RET Thyroid/Adrenal 7011 NDC 63083-7011

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-7011Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-7011Add 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
63083-7011-1	6308370110163083701101	29.5 mL in 1 BOTTLE, DROPPER (63083-7011-1)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 Thyroid/Adrenal 7011Suffix: 7011
Generic name (nonproprietary): ret thyroid/adrenal
Active ingredients: Populus tremula flowering top — 3 [hp_X]/29.5mLScleranthus annuus flowering top — 3 [hp_X]/29.5mLCalcium sulfate anhydrous — 3 [hp_X]/29.5mLMagnesium phosphate, Dibasic trihydrate — 3 [hp_X]/29.5mLSilicon dioxide — 3 [hp_X]/29.5mLStrychnos ignatii seed — 30 [hp_X]/29.5mLIodine — 30 [hp_X]/29.5mLLycopodium clavatum spore — 30 [hp_X]/29.5mLNutmeg — 30 [hp_X]/29.5mLSmilax ornata root — 30 [hp_X]/29.5mLZinc — 30 [hp_X]/29.5mL
Dosage form: Liquid
Route: Oral
Labeler: Professional Complementary Health FormulasNDC labeler code 63083
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)Calcium (Chemical structure)Divalent (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Food Additives (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Increased Histamine Release (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)Phosphate Chelating Activity (Mechanism)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 63083-7011_6b358381-0841-4564-98d3-f250b83c8736SPL ID 6b358381-0841-4564-98d3-f250b83c8736SPL set ID eb313eb9-4dfc-402e-92b3-14f09f4ba869UNII 5Q01F7TPJJ, CC4B5WU2XX, E934B3V59H, HF539G9L3Q, ETJ7Z6XBU4, 1NM3M2487K, 9679TC07X4, C88X29Y479, AEE24M3MQ9, 2H1576D5WG, J41CSQ7QDS
Pharmacologic class: Blood Coagulation Factor; Calculi Dissolution Agent; Non-Standardized Food Allergenic Extract; Non-Standardized Plant Allergenic Extract; Osmotic Laxative; Phosphate Binder

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

N463083701101 followed by a unit qualifier and the quantity

Package 63083-7011-01. 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 indecision, uncertainty, fear and worry of the unknown, anxiousness, or oversensitivity.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63083-7011

What is NDC 63083-7011?: 63083-7011 is the product NDC for RET Thyroid/Adrenal 7011 (ret thyroid/adrenal), Populus tremula flowering top 3 [hp_X]/29.5mL + 10 more ingredients liquid, listed with the FDA by Professional Complementary Health Formulas. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: RET Thyroid/Adrenal 7011 (RET Thyroid/Adrenal).
What is the active ingredient?: Populus tremula flowering top, Scleranthus annuus flowering top, Calcium sulfate anhydrous, Magnesium phosphate, Dibasic trihydrate, Silicon dioxide, Strychnos ignatii seed, Iodine, Lycopodium clavatum spore, Nutmeg, Smilax ornata root, Zinc.
Who is the labeler?: Professional Complementary Health Formulas, NDC labeler code 63083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for RET Thyroid/Adrenal 7011?: 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.

RET Thyroid/Adrenal 7011 (Ret thyroid/adrenal) NDC 63083-7011