Acne HP NDC 43857-0275

NDC codes

FDA NDC Directory

Product NDC (as listed)43857-0275Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43857-0275Add 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
43857-0275-1	43857027501	30 mL in 1 BOTTLE, DROPPER (43857-0275-1)Marketed from Jun 20, 2017

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 HPSuffix: HP
Generic name (nonproprietary): carbo animalis, carbo vegetabilis, kali bichromicum, natrum muriaticum, pulsatilla (vulgaris), sepia, silicea, sulphur, zincum metallicum
Active ingredients: Carbo animalis — 30 [hp_X]/mLActivated charcoal — 30 [hp_X]/mLPotassium dichromate — 30 [hp_X]/mLSodium chloride — 30 [hp_X]/mLPulsatilla vulgaris whole — 30 [hp_X]/mLSepia officinalis juice — 30 [hp_X]/mLSilicon dioxide — 30 [hp_X]/mLSulfur — 30 [hp_X]/mLZinc — 30 [hp_X]/mL
Dosage form: Liquid
Route: Oral
Labeler: BioActive Nutritional, Inc.
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Aug 4, 2014
Listing expires: Dec 31, 2027
Identifiers: Product ID 43857-0275_796f74e5-7250-4796-b678-dbde38ef6326SPL ID 796f74e5-7250-4796-b678-dbde38ef6326SPL set ID 2ab4ff53-4274-40c7-b05c-44d918d809beUNII 279O8I0433, 2P3VWU3H10, T4423S18FM, 451W47IQ8X, I76KB35JEV, QDL83WN8C2, ETJ7Z6XBU4, 70FD1KFU70, J41CSQ7QDSUPC 0210184341411

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

N443857027501 followed by a unit qualifier and the quantity

Package 43857-0275-01. 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 Mar 31, 2026.

Indications (excerpt from the label)

USES: For temporary relief of eruptions due to acne.** **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)