What is NDC 71753-2013?

71753-2013 is the product NDC for Allergy Escape, Onion 8 [hp_X]/mL + 7 more ingredients spray, listed with the FDA by Ratis, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Allergy Escape (Allium Cepa, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Urtica Urens, Wyethia Helenioides, Histaminum Hydrochloricum).

What is the active ingredient?

Onion, Euphrasia stricta, Potassium iodide, Naphthalene, Schoenocaulon officinale seed, Urtica urens whole, Wyethia helenioides root, Histamine dihydrochloride.

Ratis, LLC, NDC labeler code 71753. 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 Escape?

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 Escape NDC 71753-2013 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71753-2013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71753-2013Add 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
71753-2013-1	7175320130171753201301	30 mL in 1 BOTTLE, SPRAY (71753-2013-1)Marketed from Jul 12, 2023

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 Escape
Generic name (nonproprietary): allium cepa, euphrasia officinalis, kali iodatum, naphthalinum, sabadilla, urtica urens, wyethia helenioides, histaminum hydrochloricum
Active ingredients: Onion — 8 [hp_X]/mLEuphrasia stricta — 8 [hp_X]/mLPotassium iodide — 8 [hp_X]/mLNaphthalene — 8 [hp_X]/mLSchoenocaulon officinale seed — 8 [hp_X]/mLUrtica urens whole — 8 [hp_X]/mLWyethia helenioides root — 8 [hp_X]/mLHistamine dihydrochloride — 12 [hp_X]/mL
Dosage form: Spray
Route: Oral
Labeler: Ratis, LLCNDC labeler code 71753
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jul 12, 2023
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 71753-2013_56e85885-a836-4a35-af69-831bd90422c7SPL ID 56e85885-a836-4a35-af69-831bd90422c7SPL set ID 8bd9b9da-570a-4875-a5de-963155f0f837UNII 492225Q21H, C9642I91WL, 1C4QK22F9J, 2166IN72UN, 6NAF1689IO, IHN2NQ5OF9, J10PD1AQ0N, 3POA0Q644UUPC 0371753201311
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

N471753201301 followed by a unit qualifier and the quantity

Package 71753-2013-01. 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 Jul 12, 2023.

Indications (excerpt from the label)

USES: May temporarily relieve seasonal and environmental allergies such as runny nose, itchy eyes, sinus pressure, and puffy skin.* * 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 71753-2013

What is NDC 71753-2013?: 71753-2013 is the product NDC for Allergy Escape, Onion 8 [hp_X]/mL + 7 more ingredients spray, listed with the FDA by Ratis, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Allergy Escape (Allium Cepa, Euphrasia Officinalis, Kali Iodatum, Naphthalinum, Sabadilla, Urtica Urens, Wyethia Helenioides, Histaminum Hydrochloricum).
What is the active ingredient?: Onion, Euphrasia stricta, Potassium iodide, Naphthalene, Schoenocaulon officinale seed, Urtica urens whole, Wyethia helenioides root, Histamine dihydrochloride.
Who is the labeler?: Ratis, LLC, NDC labeler code 71753. 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 Escape?: 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.