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  4. NDC Product Code: 63083-6033 Travel Immunization Detox 6033

NDC 63083-6033 Travel Immunization Detox 6033

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63083-6033?
  4. Travel Immunization Detox 6033 Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
63083-6033
Proprietary Name:
Travel Immunization Detox 6033
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Professional Complementary Health Formulas
Labeler Code:
63083
Product Label ID:
b74abfad-fe22-476c-9692-07d66cc15ac5
Start Marketing Date: [9]
08-15-1984
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 63083-6033?

The NDC code 63083-6033 is assigned by the FDA to the product Travel Immunization Detox 6033 which is product labeled by Professional Complementary Health Formulas. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63083-6033-2 59 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Travel Immunization Detox 6033?

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.*

Which are Travel Immunization Detox 6033 UNII Codes?

The UNII codes for the active ingredients in this product are:

  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8)
  • ECHINACEA ANGUSTIFOLIA WHOLE (UNII: VB06AV5US8) (Active Moiety)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
  • SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786)
  • THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (Active Moiety)
  • ARSENIC TRIOXIDE (UNII: S7V92P67HO)
  • ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
  • SULFUR (UNII: 70FD1KFU70)
  • SULFUR (UNII: 70FD1KFU70) (Active Moiety)
  • MELANDRIN (UNII: C7UC00UZ0I)
  • MELANDRIN (UNII: C7UC00UZ0I) (Active Moiety)
  • CHOLERA ENTEROTOXIN SUBUNIT B (UNII: 1FKD81GIZJ)
  • CHOLERA ENTEROTOXIN SUBUNIT B (UNII: 1FKD81GIZJ) (Active Moiety)
  • HEPATITIS A VIRUS STRAIN HM175 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 5BFC8LZ6LQ)
  • HEPATITIS A VIRUS STRAIN HM175 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 5BFC8LZ6LQ) (Active Moiety)
  • JAPANESE ENCEPHALITIS VIRUS STRAIN NAKAYAMA-NIH ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 2V2JJ0S00T)
  • JAPANESE ENCEPHALITIS VIRUS STRAIN NAKAYAMA-NIH ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 2V2JJ0S00T) (Active Moiety)
  • ANOPHELES QUADRIMACULATUS (UNII: B4ULB6ARCO)
  • ANOPHELES QUADRIMACULATUS (UNII: B4ULB6ARCO) (Active Moiety)
  • MUMPS VIRUS (UNII: YF0S03R447)
  • MUMPS VIRUS (UNII: YF0S03R447) (Active Moiety)
  • POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 0LVY784C09)
  • POLIOVIRUS TYPE 1 ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: 0LVY784C09) (Active Moiety)
  • CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K3W1N8YP13)
  • CLOSTRIDIUM TETANI TOXOID ANTIGEN (FORMALDEHYDE INACTIVATED) (UNII: K3W1N8YP13) (Active Moiety)
  • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O)
  • SALMONELLA ENTERICA ENTERICA SEROVAR TYPHI (UNII: 760T5R8B3O) (Active Moiety)
  • YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN (UNII: PY4EET359T)
  • YELLOW FEVER VIRUS STRAIN 17D-204 LIVE ANTIGEN (UNII: PY4EET359T) (Active Moiety)

Which are Travel Immunization Detox 6033 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".