What is NDC 63083-6033?

63083-6033 is the product NDC for Travel Immunization Detox 6033 (travel immunization detox), Oyster shell calcium carbonate, Crude 3 [hp_X]/59mL + 15 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?

Travel Immunization Detox 6033 (Travel Immunization Detox).

What is the active ingredient?

Oyster shell calcium carbonate, Crude, Echinacea angustifolia whole, Silicon dioxide, Thuja occidentalis leaf, Arsenic trioxide, Sulfur, Melandrin, Cholera enterotoxin subunit b, Hepatitis a virus strain hm175 antigen (Formaldehyde inactivated), Japanese encephalitis virus strain nakayama-nih antigen (Formaldehyde inactivated), Anopheles quadrimaculatus, Mumps virus, Poliovirus type 1 antigen (Formaldehyde inactivated), Clostridium tetani toxoid antigen (Formaldehyde inactivated), Salmonella enterica enterica serovar typhi, Yellow fever virus strain 17d-204 live antigen.

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 Travel Immunization Detox 6033?

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.

Travel Immunization Detox 6033 NDC 63083-6033

NDC codes

FDA NDC Directory

Product NDC (as listed)63083-6033Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63083-6033Add 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
63083-6033-2	6308360330263083603302	59 mL in 1 BOTTLE, DROPPER (63083-6033-2)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): Travel Immunization Detox 6033Suffix: 6033
Generic name (nonproprietary): travel 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]/59mLCholera enterotoxin subunit b — 12 [hp_X]/59mLHepatitis a virus strain hm175 antigen (Formaldehyde inactivated) — 12 [hp_X]/59mLJapanese encephalitis virus strain nakayama-nih antigen (Formaldehyde inactivated) — 12 [hp_X]/59mLAnopheles quadrimaculatus — 12 [hp_X]/59mLMumps virus — 12 [hp_X]/59mLPoliovirus type 1 antigen (Formaldehyde inactivated) — 12 [hp_X]/59mLClostridium tetani toxoid antigen (Formaldehyde inactivated) — 12 [hp_X]/59mLSalmonella enterica enterica serovar typhi — 12 [hp_X]/59mLYellow fever virus strain 17d-204 live antigen — 12 [hp_X]/59mL
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: Actively Acquired Immunity (Physiologic effect)Actively Acquired Immunity (Physiologic effect)Actively Acquired Immunity (Physiologic effect)Actively Acquired Immunity (Physiologic effect)Actively Acquired Immunity (Physiologic effect)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Hepatitis A Vaccines (Chemical structure)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Insect Proteins (Chemical structure)Japanese Encephalitis Vaccines (Chemical structure)Poliovirus Vaccines (Chemical structure)Tetanus Toxoid (Chemical structure)Attenuated (Chemical structure)Inactivated (Chemical structure)Inactivated (Chemical structure)Inactivated (Chemical structure)Inactivated (Chemical structure)Yellow Fever Vaccine (Chemical structure)
Identifiers: Product ID 63083-6033_1883594f-f47d-4463-8715-fd18d37deb1cSPL ID 1883594f-f47d-4463-8715-fd18d37deb1cSPL set ID b74abfad-fe22-476c-9692-07d66cc15ac5UNII 2E32821G6I, VB06AV5US8, ETJ7Z6XBU4, 0T0DQN8786, S7V92P67HO, 70FD1KFU70, C7UC00UZ0I, 1FKD81GIZJ, 5BFC8LZ6LQ, 2V2JJ0S00T, B4ULB6ARCO, YF0S03R447, 0LVY784C09, K3W1N8YP13, 760T5R8B3O, PY4EET359T
Pharmacologic class: Inactivated Clostridium Tetani Vaccine; Inactivated Hepatitis A Virus Vaccine; Inactivated Japanese Encephalitis Virus Vaccine; Inactivated Poliovirus Vaccine; Live Attenuated Yellow Fever Virus Vaccine; Non-Standardized Insect 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.

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

N463083603302 followed by a unit qualifier and the quantity

Package 63083-6033-02. 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 aches, pains, or stiffness of muscles or joints, occasional headache, tiredness, chills, mild itching, 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)

About NDC 63083-6033

What is NDC 63083-6033?: 63083-6033 is the product NDC for Travel Immunization Detox 6033 (travel immunization detox), Oyster shell calcium carbonate, Crude 3 [hp_X]/59mL + 15 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?: Travel Immunization Detox 6033 (Travel Immunization Detox).
What is the active ingredient?: Oyster shell calcium carbonate, Crude, Echinacea angustifolia whole, Silicon dioxide, Thuja occidentalis leaf, Arsenic trioxide, Sulfur, Melandrin, Cholera enterotoxin subunit b, Hepatitis a virus strain hm175 antigen (Formaldehyde inactivated), Japanese encephalitis virus strain nakayama-nih antigen (Formaldehyde inactivated), Anopheles quadrimaculatus, Mumps virus, Poliovirus type 1 antigen (Formaldehyde inactivated), Clostridium tetani toxoid antigen (Formaldehyde inactivated), Salmonella enterica enterica serovar typhi, Yellow fever virus strain 17d-204 live antigen.
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 Travel Immunization Detox 6033?: 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.

Travel Immunization Detox 6033 (Travel immunization detox) NDC 63083-6033