What is NDC 57955-9997?

57955-9997 is the product NDC for Allergy Relief Indoor and Outdoor, Onion 10 [hp_X]/59mL + 16 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Allergy Relief Indoor and Outdoor (Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali bichromicum, Naphthalinum, Natrum muriaticum, Sabadilla, Solidago virgaurea, Sticta pulmonaria, Sulphur, Trifolium pratense, and Wyethia helenioides.).

What is the active ingredient?

Onion, Ambrosia artemisiifolia whole, Arsenic trioxide, Arisaema triphyllum root, Arundo pliniana root, Euphrasia stricta, Galphimia glauca flowering top, Histamine dihydrochloride, Potassium dichromate, Naphthalene, Sodium chloride, Schoenocaulon officinale seed, Solidago virgaurea flowering top, Lobaria pulmonaria, Sulfur, Trifolium pratense flower, Wyethia helenioides root.

King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Allergy Relief Indoor and Outdoor?

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.

Allergy Relief Indoor and Outdoor NDC 57955-9997

NDC codes

FDA NDC Directory

Product NDC (as listed)57955-9997Labeler and product segments. Claims need a package NDC.

Product NDC at billing width57955-9997Add 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
57955-9997-2	5795599970257955999702	59 mL in 1 BOTTLE, SPRAY (57955-9997-2)Marketed from Oct 20, 2025

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): Allergy Relief Indoor and Outdoor
Generic name (nonproprietary): allium cepa, ambrosia artemisiaefolia, arsenicum album, arum triphyllum, arundo mauritanica, euphrasia officinalis, galphimia glauca, histaminum hydrochloricum, kali bichromicum, naphthalinum, natrum muriaticum, sabadilla, solidago virgaurea, sticta pulmonaria, sulphur, trifolium pratense, and wyethia helenioides.
Active ingredients: Onion — 10 [hp_X]/59mLAmbrosia artemisiifolia whole — 10 [hp_X]/59mLArsenic trioxide — 10 [hp_X]/59mLArisaema triphyllum root — 10 [hp_X]/59mLArundo pliniana root — 10 [hp_X]/59mLEuphrasia stricta — 10 [hp_X]/59mLGalphimia glauca flowering top — 10 [hp_X]/59mLHistamine dihydrochloride — 10 [hp_X]/59mLPotassium dichromate — 10 [hp_X]/59mLNaphthalene — 10 [hp_X]/59mLSodium chloride — 10 [hp_X]/59mLSchoenocaulon officinale seed — 10 [hp_X]/59mLSolidago virgaurea flowering top — 10 [hp_X]/59mLLobaria pulmonaria — 10 [hp_X]/59mLSulfur — 10 [hp_X]/59mLTrifolium pratense flower — 10 [hp_X]/59mLWyethia helenioides root — 10 [hp_X]/59mL
Dosage form: Liquid
Route: Oral
Labeler: King Bio Inc.NDC labeler code 57955
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Oct 20, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Dietary Proteins (Chemical structure)Increased Histamine Release (Physiologic effect)Vegetable Proteins (Chemical structure)
Identifiers: Product ID 57955-9997_ead77196-04d9-4de5-922c-7be79ecce52bSPL ID ead77196-04d9-4de5-922c-7be79ecce52bSPL set ID 9faa963e-4ddc-461f-95a1-2d10e1260612UNII 492225Q21H, 9W34L2CQ9A, S7V92P67HO, DM64K844DM, ZXE7LB03WC, C9642I91WL, 93PH5Q8M7E, 3POA0Q644U, T4423S18FM, 2166IN72UN, 451W47IQ8X, 6NAF1689IO, 5405K23S50, D1YM0P5Z2T, 70FD1KFU70, 4JS0838828, J10PD1AQ0N
Pharmacologic class: Non-Standardized Food 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

N457955999702 followed by a unit qualifier and the quantity

Package 57955-9997-02. 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 Mar 2, 2026.

Indications (excerpt from the label)

Uses † for temporary relief of: common hay fever and household allergies nasal sinus throat mucus congestion runny nose sneezing cough red itchy or watery eyes respiratory difficulties skin irritations headaches † Claims based on traditional Homeopathic practice, not accepted medical evidence, not FDA evaluated.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 57955-9997

What is NDC 57955-9997?: 57955-9997 is the product NDC for Allergy Relief Indoor and Outdoor, Onion 10 [hp_X]/59mL + 16 more ingredients liquid, listed with the FDA by King Bio Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Allergy Relief Indoor and Outdoor (Allium cepa, Ambrosia artemisiaefolia, Arsenicum album, Arum triphyllum, Arundo mauritanica, Euphrasia officinalis, Galphimia glauca, Histaminum hydrochloricum, Kali bichromicum, Naphthalinum, Natrum muriaticum, Sabadilla, Solidago virgaurea, Sticta pulmonaria, Sulphur, Trifolium pratense, and Wyethia helenioides.).
What is the active ingredient?: Onion, Ambrosia artemisiifolia whole, Arsenic trioxide, Arisaema triphyllum root, Arundo pliniana root, Euphrasia stricta, Galphimia glauca flowering top, Histamine dihydrochloride, Potassium dichromate, Naphthalene, Sodium chloride, Schoenocaulon officinale seed, Solidago virgaurea flowering top, Lobaria pulmonaria, Sulfur, Trifolium pratense flower, Wyethia helenioides root.
Who is the labeler?: King Bio Inc., NDC labeler code 57955. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allergy Relief Indoor and Outdoor?: 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.