Childhood Immunization Detox 6032 NDC 63083-6032

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6032Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6032Add 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
63083-6032-2	63083603202	59 mL in 1 BOTTLE, DROPPER (63083-6032-2)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): Childhood Immunization Detox 6032Suffix: 6032
Generic name (nonproprietary): childhood immunization detox
Active ingredients: Oyster shell calcium carbonate, Crude — 3 [hp_X]/59mLEchinacea angustifolia whole — 3 [hp_X]/59mLSilicon dioxide — 3 [hp_X]/59mLThuja occidentalis leaf — 3 [hp_X]/59mLArsenic trioxide — 6 [hp_X]/59mLSulfur — 6 [hp_X]/59mLMelandrin — 30 [hp_X]/59mLL-3972-t — 60 [hp_X]/59mLHepatitis a virus strain hm175 antigen (Formaldehyde inactivated) — 60 [hp_X]/59mLMycobacterium bovis bcg — 60 [hp_X]/59mLMumps virus — 60 [hp_X]/59mLClostridium tetani toxoid antigen (Formaldehyde inactivated) — 60 [hp_X]/59mLHuman varicella-zoster immune globulin — 60 [hp_X]/59mL
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: Actively Acquired Immunity (Physiologic effect)Actively Acquired Immunity (Physiologic effect)Hepatitis A Vaccines (Chemical structure)Tetanus Toxoid (Chemical structure)Inactivated (Chemical structure)Inactivated (Chemical structure)
Identifiers: Product ID 63083-6032_8cafa58e-f0ee-4ef1-8fe9-48f3df6a8a76SPL ID 8cafa58e-f0ee-4ef1-8fe9-48f3df6a8a76SPL set ID 4d455d07-3197-44d6-99d6-488fcdb50f95UNII 2E32821G6I, VB06AV5US8, ETJ7Z6XBU4, 0T0DQN8786, S7V92P67HO, 70FD1KFU70, C7UC00UZ0I, 06HG6YW0HK, 5BFC8LZ6LQ, D3GOY6203T, YF0S03R447, K3W1N8YP13, 33T61IWL27
Pharmacologic class: Inactivated Clostridium Tetani Vaccine; Inactivated Hepatitis A Virus Vaccine

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.

Administration

Immunization administration (CPT 90460–90474)

Giving a vaccine is reported separately from the vaccine product code, with an immunization administration code. Which code applies depends on the patient's age, the route and whether counselling was provided.

How CPT relates to drug billing

NDC on a medical claim

N463083603202 followed by a unit qualifier and the quantity

Package 63083-6032-02. 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 Jan 8, 2026.

Indications (excerpt from the label)

INDICATIONS For the temporary relief of fussiness, tiredness, loss of appetite, minor aches or pains, occasional headache, nausea, or vomiting due to sensitivity to vaccination.*

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)