Acne Tonic NDC 61096-1027

NDC codes

FDA NDC Directory

Product NDC (as listed)61096-1027Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61096-1027Add 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
61096-1027-1	61096102701	1 BOTTLE, SPRAY in 1 CARTON (61096-1027-1) / 41 mL in 1 BOTTLE, SPRAYMarketed from Mar 8, 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): Acne Tonic
Generic name (nonproprietary): anthracinum, antimonium crud, apis mel, carbo an, hamamelis, hepar suis, hydrocotyle, kali brom, merc corros, nat sulphuricum, pyrogenium, radium brom, sanguinaria canadensis, sulphur iod, thuja occ, urtica ur
Active ingredients: Bacillus anthracis immunoserum rabbit — 200 [hp_C]/41mLAntimony trisulfide — 30 [hp_C]/41mLApis mellifera — 4 [hp_X]/41mLCarbo animalis — 12 [hp_X]/41mLHamamelis virginiana root bark/stem bark — 4 [hp_X]/41mLPork liver — 6 [hp_X]/41mLCentella asiatica whole — 30 [hp_C]/41mLPotassium bromide — 30 [hp_C]/41mLMercuric chloride — 200 [hp_C]/41mLSodium sulfide nonahydrate — 200 [hp_C]/41mLRancid beef — 30 [hp_C]/41mLRadium bromide — 200 [hp_C]/41mLSanguinaria canadensis root — 4 [hp_X]/41mLSulfur iodide — 200 [hp_C]/41mLThuja occidentalis leafy twig — 200 [hp_C]/41mLUrtica urens whole — 4 [hp_X]/41mL
Dosage form: Liquid
Route: Oral
Labeler: Eight and Company L.L.C
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 8, 2019
Listing expires: Dec 31, 2026
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)Osmotic Activity (Mechanism)
Identifiers: Product ID 61096-1027_2796c451-737e-4bdc-8fff-f0565ff0a16cSPL ID 2796c451-737e-4bdc-8fff-f0565ff0a16cSPL set ID bb635329-47ce-47a5-b18d-124d58a03e79UNII 41LZ22DD4N, F79059A38U, 7S82P3R43Z, 279O8I0433, T7S323PKJS, 6EC706HI7F, 7M867G6T1U, OSD78555ZM, 53GH7MZT1R, C02T02993U, 29SUH5R3HU, R74O7T8569, N9288CD508, L6L8KA2AA0, 1NT28V9397, IHN2NQ5OF9UPC 0361096002713
Pharmacologic class: Osmotic Laxative; 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

N461096102701 followed by a unit qualifier and the quantity

Package 61096-1027-01. 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 18, 2025.

Indications (excerpt from the label)

INDICATIONS: Temporarily relieves acne discomfort and the common symptoms of acne, including: ° Face and body breakouts ° redness ° itching and inflammation ° 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)