Over-the-counter drug · UNAPPROVED HOMEOPATHIC
Systemic Detox NDC 43742-2141
Beta vulgaris whole 12 [hp_X]/mL + 13 more ingredients · Liquid · Oral · Deseret Biologicals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 43742-2141-1 | 43742214101 | 30 mL in 1 BOTTLE, DROPPER (43742-2141-1)Marketed from Mar 13, 2024 |
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)
- Systemic Detox
- Generic name (nonproprietary)
- beta vulgaris, boldo, chelidonium majus, ferrum metallicum, gelsemium sempervirens, iodium, lycopodium clavatum, nux vomica, pulsatilla (pratensis), sarsaparilla (smilax regelii), selenium metallicum, thuja occidentalis, veratrum album, zincum metallicum
- Active ingredients
- Beta vulgaris whole — 12 [hp_X]/mLPeumus boldus leaf — 3 [hp_X]/mLChelidonium majus whole — 3 [hp_X]/mLIron — 12 [hp_X]/mLGelsemium sempervirens root — 8 [hp_X]/mLIodine — 12 [hp_X]/mLLycopodium clavatum spore — 12 [hp_X]/mLStrychnos nux-vomica seed — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSmilax ornata root — 6 [hp_X]/mLSelenium — 12 [hp_X]/mLThuja occidentalis leafy twig — 12 [hp_X]/mLVeratrum album root — 8 [hp_X]/mLZinc — 12 [hp_X]/mL
- Dosage form
- Liquid
- Route
- Oral
- Labeler
- Deseret Biologicals, Inc.
- Product type
- Over-the-counter drug
- Marketing category
- Unapproved homeopathic
- Marketing start
- Listing expires
- Other FDA classes
- Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
- Identifiers
- Product ID 43742-2141_0fecbbd1-14db-43b5-b41b-cc96eeab01c3SPL ID 0fecbbd1-14db-43b5-b41b-cc96eeab01c3SPL set ID 7ef75c3f-2d34-4822-8b94-8bce88709afdUNII 4G174V5051, Q4EWM09M3O, 7E889U5RNN, E1UOL152H7, 639KR60Q1Q, 9679TC07X4, C88X29Y479, 269XH13919, 8E272251DI, 2H1576D5WG, H6241UJ22B, 1NT28V9397, QNS6W5US1Z, J41CSQ7QDSUPC 0810151880716
- Pharmacologic class
- Non-Standardized Plant 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
N443742214101followed by a unit qualifier and the quantityPackage 43742-2141-01. 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 .
Indications (excerpt from the label)
USES: • For the temporary relief of symptoms including: • bladder discomfort • perspiration • expectoration • nasal discomfort • mucus congestion • occasional constipation These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.
Excerpt only. Read the full label for complete information.