Household Antigens NDC 44911-0725

NDC codes

FDA NDC Directory

Product NDC (as listed)44911-0725Labeler and product segments. Claims need a package NDC.

Product NDC at billing width44911-0725Add 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
44911-0725-1	44911072501	30 mL in 1 BOTTLE, DROPPER (44911-0725-1)Marketed from Dec 20, 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): Household Antigens
Generic name (nonproprietary): acetone, sodium tripolyphosphate, propylene glycol, benzinum, ammonium muriaticum, sodium lauryl sulfate, terebinthina, butyl acetate, ethyl acetate, toluene, xylene, bisphenol a, petroleum, formalinum, glyphosate, methylparaben, naphthalinum, propylparaben, anacardium orientale, graphites, nitricum acidum, pulsatilla (pratensis), sulphur, paraffinum
Active ingredients: Acetone — 9 [hp_X]/mLSodium tripolyphosphate, Unspecified form — 9 [hp_X]/mLPropylene glycol — 9 [hp_X]/mLBenzene — 9 [hp_X]/mLAmmonium chloride — 9 [hp_X]/mLSodium lauryl sulfate — 9 [hp_X]/mLTurpentine oil — 9 [hp_X]/mLButyl acetate — 9 [hp_X]/mLEthyl acetate — 9 [hp_X]/mLToluene — 9 [hp_X]/mLXylene (Mixed isomers) — 9 [hp_X]/mLBisphenol a — 9 [hp_X]/mLKerosene — 9 [hp_X]/mLFormaldehyde solution — 9 [hp_X]/mLGlyphosate — 9 [hp_X]/mLMethylparaben — 9 [hp_X]/mLNaphthalene — 9 [hp_X]/mLPropylparaben — 9 [hp_X]/mLSemecarpus anacardium juice — 12 [hp_X]/mLGraphite — 12 [hp_X]/mLNitric acid — 12 [hp_X]/mLPulsatilla pratensis whole — 12 [hp_X]/mLSulfur — 12 [hp_X]/mLParaffin — 12 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: Energique, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Dec 20, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)
Identifiers: Product ID 44911-0725_037a3c93-3157-4424-a28d-b8445eb46d6eSPL ID 037a3c93-3157-4424-a28d-b8445eb46d6eSPL set ID f3db63df-62a4-48d6-92e7-94e4a5701552UNII 1364PS73AF, 5HK03SA80J, 6DC9Q167V3, J64922108F, 01Q9PC255D, 368GB5141J, C5H0QJ6V7F, 464P5N1905, 76845O8NMZ, 3FPU23BG52, D856J1047R, MLT3645I99, 1C89KKC04E, T0H3L6C7I5, 4632WW1X5A, A2I8C7HI9T, 2166IN72UN, Z8IX2SC1OH, Y0F0BU8RDU, 4QQN74LH4O, 411VRN1TV4, 8E272251DI, 70FD1KFU70, I9O0E3H2ZEUPC 0363113700435
Pharmacologic class: Standardized Chemical Allergen

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

N444911072501 followed by a unit qualifier and the quantity

Package 44911-0725-01. 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 Dec 20, 2024.

Indications (excerpt from the label)

INDICATIONS: May temporarily relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.** **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)