What is NDC 61096-2007?

61096-2007 is the product NDC for Sprayology TravelEase, Milk thistle 4 [hp_X]/41mL + 7 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Sprayology TravelEase (Apis mel, Carbo veg, Carduus mar, Cocculus, Ignatia, Nux vom, Passiflora, Tabacum).

What is the active ingredient?

Milk thistle, Anamirta cocculus seed, Strychnos ignatii seed, Strychnos nux-vomica seed, Passiflora incarnata flowering top, Tobacco leaf, Apis mellifera, Activated charcoal.

Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sprayology TravelEase?

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.

Sprayology TravelEase NDC 61096-2007

NDC codes

FDA NDC Directory

Product NDC (as listed)61096-2007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61096-2007Add 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
61096-2007-1	6109620070161096200701	1 BOTTLE, SPRAY in 1 CARTON (61096-2007-1) / 41 mL in 1 BOTTLE, SPRAYMarketed from Feb 12, 2019

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): Sprayology TravelEase
Generic name (nonproprietary): apis mel, carbo veg, carduus mar, cocculus, ignatia, nux vom, passiflora, tabacum
Active ingredients: Milk thistle — 4 [hp_X]/41mLAnamirta cocculus seed — 30 [hp_C]/41mLStrychnos ignatii seed — 200 [hp_C]/41mLStrychnos nux-vomica seed — 30 [hp_C]/41mLPassiflora incarnata flowering top — 4 [hp_X]/41mLTobacco leaf — 6 [hp_X]/41mLApis mellifera — 200 [hp_C]/41mLActivated charcoal — 200 [hp_C]/41mL
Dosage form: Liquid
Route: Oral
Labeler: Eight and Company L.L.CNDC labeler code 61096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Feb 12, 2019
Listing expires: Dec 31, 2026
Other FDA classes: Allergens (Chemical structure)Allergens (Chemical structure)Allergens (Chemical structure)Bee Venoms (Chemical structure)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Cell-mediated Immunity (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased Histamine Release (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Increased IgG Production (Physiologic effect)Plant Proteins (Chemical structure)Plant Proteins (Chemical structure)Seed Storage Proteins (Chemical structure)
Identifiers: Product ID 61096-2007_25ae622f-4467-4b1f-a3ed-cbcf8e412336SPL ID 25ae622f-4467-4b1f-a3ed-cbcf8e412336SPL set ID 104c72b0-2892-4262-81b8-7f7f0184615aUNII U946SH95EE, 810258W28U, 1NM3M2487K, 269XH13919, CLF5YFS11O, 6YR2608RSU, 7S82P3R43Z, 2P3VWU3H10
Pharmacologic class: Non-Standardized Plant Allergenic Extract; Standardized Insect Venom 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

N461096200701 followed by a unit qualifier and the quantity

Package 61096-2007-01. 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 24, 2025.

Indications (excerpt from the label)

For use during and after jet travel to temporarily relieve the symptoms commonly known as "jet lag", including: ° tiredness ° dehydration ° feeling of disorientation ° sleeplessness -natural -gluten & lactose free -no artificial flavors or colors -no known negative side effects -no known negative drug interactions

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 61096-2007

What is NDC 61096-2007?: 61096-2007 is the product NDC for Sprayology TravelEase, Milk thistle 4 [hp_X]/41mL + 7 more ingredients liquid, listed with the FDA by Eight and Company L.L.C. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sprayology TravelEase (Apis mel, Carbo veg, Carduus mar, Cocculus, Ignatia, Nux vom, Passiflora, Tabacum).
What is the active ingredient?: Milk thistle, Anamirta cocculus seed, Strychnos ignatii seed, Strychnos nux-vomica seed, Passiflora incarnata flowering top, Tobacco leaf, Apis mellifera, Activated charcoal.
Who is the labeler?: Eight and Company L.L.C, NDC labeler code 61096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sprayology TravelEase?: 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.