What is NDC 62630-003?

62630-003 is the product NDC for PreQuimm, Silver nitrate 6 [hp_X]/1 + 6 more ingredients tablet, listed with the FDA by ZRG Detox, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

PreQuimm (Silver nitrate,colchicum autumnale bulb,conium maculatum flowering top,ipecac,strychnos nux vomica seed,pulsatilla pratensis whole,veratrum album root).

What is the active ingredient?

Silver nitrate, Colchicum autumnale bulb, Conium maculatum flowering top, Ipecac, Strychnos nux-vomica seed, Pulsatilla pratensis whole, Veratrum album root.

ZRG Detox, Inc., NDC labeler code 62630. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for PreQuimm?

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.

PreQuimm NDC 62630-003 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62630-003Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62630-0003Add 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
62630-003-01	6263000030162630000301	100 TABLET in 1 BOTTLE (62630-003-01)Marketed from Oct 15, 2024

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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): PreQuimm
Generic name (nonproprietary): silver nitrate,colchicum autumnale bulb,conium maculatum flowering top,ipecac,strychnos nux vomica seed,pulsatilla pratensis whole,veratrum album root
Active ingredients: Silver nitrate — 6 [hp_X]/1Colchicum autumnale bulb — 4 [hp_X]/1Conium maculatum flowering top — 4 [hp_X]/1Ipecac — 4 [hp_X]/1Strychnos nux-vomica seed — 5 [hp_X]/1Pulsatilla pratensis whole — 6 [hp_X]/1Veratrum album root — 8 [hp_X]/1
Dosage form: Tablet
Route: Sublingual
Labeler: ZRG Detox, Inc.NDC labeler code 62630
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 15, 2024
Listing expires: Dec 31, 2026
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 62630-003_42246a7e-5f14-68c0-e063-6394a90af8c6SPL ID 42246a7e-5f14-68c0-e063-6394a90af8c6SPL set ID 6db848aa-bf72-466e-8bc8-d02d073ed120UNII 95IT3W8JZE, 993QHL78E6, Q28R5GF371, 62I3C8233L, 269XH13919, 8E272251DI, QNS6W5US1Z
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. Sublingual products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N462630000301 followed by a unit qualifier and the quantity

Package 62630-0003-01. 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 Oct 27, 2025.

Indications (excerpt from the label)

INDICATIONS: Temporarily relieves side effects, digestive symptoms (colic, reflux, dyspepsia, nausea, loss of appetite, vomiting, etc.) and nervousness (anxiety, etc.) occurring with chemotherapy treatments.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62630-003

What is NDC 62630-003?: 62630-003 is the product NDC for PreQuimm, Silver nitrate 6 [hp_X]/1 + 6 more ingredients tablet, listed with the FDA by ZRG Detox, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: PreQuimm (Silver nitrate,colchicum autumnale bulb,conium maculatum flowering top,ipecac,strychnos nux vomica seed,pulsatilla pratensis whole,veratrum album root).
What is the active ingredient?: Silver nitrate, Colchicum autumnale bulb, Conium maculatum flowering top, Ipecac, Strychnos nux-vomica seed, Pulsatilla pratensis whole, Veratrum album root.
Who is the labeler?: ZRG Detox, Inc., NDC labeler code 62630. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for PreQuimm?: 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.