Acne Relief NDC 70163-0038

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0038Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0038Add 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
70163-0038-1	70163003801	1 BLISTER PACK in 1 CARTON (70163-0038-1) / 60 TABLET, CHEWABLE in 1 BLISTER PACKMarketed from May 8, 2026

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 Relief
Generic name (nonproprietary): belladonna, silicea, graphites, hepar sulphuris calcareum, kali bromatum, ledum palustre, natrum muriaticum, selenium, sulphur
Active ingredients: Atropa belladonna — 6 [hp_X]/1Silicon dioxide — 12 [hp_X]/1Graphite — 10 [hp_X]/1Calcium sulfide — 12 [hp_X]/1Potassium bromide — 12 [hp_X]/1Rhododendron tomentosum leafy twig — 6 [hp_X]/1Sodium chloride — 30 [hp_X]/1Selenium — 12 [hp_X]/1Sulfur — 6 [hp_X]/1
Dosage form: Tablet, Chewable
Route: Oral
Labeler: NaturalCare
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: May 8, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 70163-0038_52c2726d-cfe6-4c4f-8550-897d783a08a2SPL ID 52c2726d-cfe6-4c4f-8550-897d783a08a2SPL set ID 487b1373-b78c-4510-964a-6ab0fe781ff4UNII WQZ3G9PF0H, ETJ7Z6XBU4, 4QQN74LH4O, 1MBW07J51Q, OSD78555ZM, 877L01IZ0P, 451W47IQ8X, H6241UJ22B, 70FD1KFU70

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

N470163003801 followed by a unit qualifier and the quantity

Package 70163-0038-01. 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 May 8, 2026.

Indications (excerpt from the label)

USES: May help temporarily ■ clear and treat existing acne pimples ■ prevent new acne pimples from forming* *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)