What is NDC 17089-462?

17089-462 is the product NDC for Guna Lympho Detox, Apis mellifera 8 [hp_X]/30mL + 19 more ingredients solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Guna Lympho Detox (Aesculus hippocastanum - apis mellifera - calendula officinalis flower - hexaketocyclohexane - equisetum hyemale - fumaric acid - graphite - hydrastis canadensis - hydrocotyle asiatica - juglans regia - levothyroxine - magnesium phosphate - malic acid - myosotis arvensis - phytolacca americana root - sarsaparilla - sodium diethyl oxalacetate - sodium pyruvate - sus scrofa placenta - taraxacum officinale -).

What is the active ingredient?

Apis mellifera, Calendula officinalis flower, Malic acid, Equisetum hyemale, Fumaric acid, Graphite, Juglans regia fruit rind, Immature, Levothyroxine, Magnesium phosphate, Dibasic trihydrate, Myosotis arvensis, Sodium diethyl oxalacetate, Sodium pyruvate, Phytolacca americana root, Sarsaparilla, Taraxacum officinale, Dodecahydroxycyclohexane dihydrate, Sus scrofa placenta, Horse chestnut, Goldenseal, Centella asiatica whole.

Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Guna Lympho Detox?

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.

Guna Lympho Detox NDC 17089-462 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)17089-462Labeler and product segments. Claims need a package NDC.

Product NDC at billing width17089-0462Add 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
17089-462-18	1708904621817089046218	1 BOTTLE, DROPPER in 1 BOX (17089-462-18) / 30 mL in 1 BOTTLE, DROPPERMarketed from Sep 24, 2020

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): Guna Lympho Detox
Generic name (nonproprietary): aesculus hippocastanum - apis mellifera - calendula officinalis flower - hexaketocyclohexane - equisetum hyemale - fumaric acid - graphite - hydrastis canadensis - hydrocotyle asiatica - juglans regia - levothyroxine - magnesium phosphate - malic acid - myosotis arvensis - phytolacca americana root - sarsaparilla - sodium diethyl oxalacetate - sodium pyruvate - sus scrofa placenta - taraxacum officinale -
Active ingredients: Apis mellifera — 8 [hp_X]/30mLCalendula officinalis flower — 1 [hp_X]/30mLMalic acid — 6 [hp_X]/30mLEquisetum hyemale — 3 [hp_X]/30mLFumaric acid — 6 [hp_X]/30mLGraphite — 12 [hp_X]/30mLJuglans regia fruit rind, Immature — 5 [hp_X]/30mLLevothyroxine — 12 [hp_X]/30mLMagnesium phosphate, Dibasic trihydrate — 12 [hp_X]/30mLMyosotis arvensis — 4 [hp_X]/30mLSodium diethyl oxalacetate — 6 [hp_X]/30mLSodium pyruvate — 6 [hp_X]/30mLPhytolacca americana root — 4 [hp_X]/30mLSarsaparilla — 3 [hp_X]/30mLTaraxacum officinale — 1 [hp_X]/30mLDodecahydroxycyclohexane dihydrate — 6 [hp_X]/30mLSus scrofa placenta — 6 [hp_X]/30mLHorse chestnut — 2 [hp_X]/30mLGoldenseal — 5 [hp_X]/30mLCentella asiatica whole — 2 [hp_X]/30mL
Dosage form: Solution/ drops
Route: Oral
Labeler: Guna spaNDC labeler code 17089
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Sep 24, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)Thyroxine (Chemical structure)
Identifiers: Product ID 17089-462_b2588f62-6cc5-327e-e053-2a95a90aaafbSPL ID b2588f62-6cc5-327e-e053-2a95a90aaafbSPL set ID aeb71e21-2fdb-6b84-e053-2995a90a4c01UNII 7S82P3R43Z, P0M7O4Y7YD, 817L1N4CKP, 59677RXH25, 88XHZ13131, 4QQN74LH4O, ZPS7Q5U53K, Q51BO43MG4, HF539G9L3Q, C73BK97H5J, 6CA025Y4FG, POD38AIF08, 11E6VI8VEG, 2H1576D5WG, 39981FM375, 5BWD2J7B4W, C8CV8867O8, 3C18L6RJAZ, ZW3Z11D0JV, 7M867G6T1U
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative; Standardized Insect Venom Allergenic Extract; l-Thyroxine

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

N417089046218 followed by a unit qualifier and the quantity

Package 17089-0462-18. 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 23, 2020.

Indications (excerpt from the label)

Take 15 minutes before meals

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 17089-462

What is NDC 17089-462?: 17089-462 is the product NDC for Guna Lympho Detox, Apis mellifera 8 [hp_X]/30mL + 19 more ingredients solution/ drops, listed with the FDA by Guna spa. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Guna Lympho Detox (Aesculus hippocastanum - apis mellifera - calendula officinalis flower - hexaketocyclohexane - equisetum hyemale - fumaric acid - graphite - hydrastis canadensis - hydrocotyle asiatica - juglans regia - levothyroxine - magnesium phosphate - malic acid - myosotis arvensis - phytolacca americana root - sarsaparilla - sodium diethyl oxalacetate - sodium pyruvate - sus scrofa placenta - taraxacum officinale -).
What is the active ingredient?: Apis mellifera, Calendula officinalis flower, Malic acid, Equisetum hyemale, Fumaric acid, Graphite, Juglans regia fruit rind, Immature, Levothyroxine, Magnesium phosphate, Dibasic trihydrate, Myosotis arvensis, Sodium diethyl oxalacetate, Sodium pyruvate, Phytolacca americana root, Sarsaparilla, Taraxacum officinale, Dodecahydroxycyclohexane dihydrate, Sus scrofa placenta, Horse chestnut, Goldenseal, Centella asiatica whole.
Who is the labeler?: Guna spa, NDC labeler code 17089. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Guna Lympho Detox?: 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.