What is NDC 66096-747?

66096-747 is the product NDC for Acne Relief Gel, Calendula officinalis flowering top 1 [hp_X]/50g + 5 more ingredients gel, listed with the FDA by OHM PHARMA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Acne Relief Gel (Calendula Officinalis, Chamomilla, Berberis Aquafolium, Hamamelis, Hepar Sulph. Calc. , Sulphur).

What is the active ingredient?

Calendula officinalis flowering top, Matricaria chamomilla, Berberis aquifolium root bark, Hamamelis virginiana root bark/stem bark, Calcium sulfide, Sulfur.

OHM PHARMA INC., NDC labeler code 66096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Acne Relief Gel?

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.

Acne Relief Gel NDC 66096-747 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)66096-747Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66096-0747Add 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
66096-747-03	6609607470366096074703	50 g in 1 TUBE (66096-747-03)Marketed from Nov 29, 2018

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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 Gel
Generic name (nonproprietary): calendula officinalis, chamomilla, berberis aquafolium, hamamelis, hepar sulph. calc. , sulphur
Active ingredients: Calendula officinalis flowering top — 1 [hp_X]/50gMatricaria chamomilla — 1 [hp_X]/50gBerberis aquifolium root bark — 2 [hp_X]/50gHamamelis virginiana root bark/stem bark — 2 [hp_X]/50gCalcium sulfide — 6 [hp_X]/50gSulfur — 6 [hp_X]/50g
Dosage form: Gel
Route: Topical
Labeler: OHM PHARMA INC.NDC labeler code 66096
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Nov 29, 2018
Listing expires: Dec 31, 2026
Identifiers: Product ID 66096-747_d44ae412-0004-a536-e053-2a95a90af73fSPL ID d44ae412-0004-a536-e053-2a95a90af73fSPL set ID 43f669ef-2ebd-46c8-adb6-84bea30a7c0bUNII 18E7415PXQ, G0R4UBI2ZZ, VZJ9F3C3SB, T7S323PKJS, 1MBW07J51Q, 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. Topical products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N466096074703 followed by a unit qualifier and the quantity

Package 66096-0747-03. 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 29, 2021.

Indications (excerpt from the label)

USES: Temporarily relieves pimples, blemishes, redness and swelling due to simple acne. Promotes natural skin healing.**

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 66096-747

What is NDC 66096-747?: 66096-747 is the product NDC for Acne Relief Gel, Calendula officinalis flowering top 1 [hp_X]/50g + 5 more ingredients gel, listed with the FDA by OHM PHARMA INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Acne Relief Gel (Calendula Officinalis, Chamomilla, Berberis Aquafolium, Hamamelis, Hepar Sulph. Calc. , Sulphur).
What is the active ingredient?: Calendula officinalis flowering top, Matricaria chamomilla, Berberis aquifolium root bark, Hamamelis virginiana root bark/stem bark, Calcium sulfide, Sulfur.
Who is the labeler?: OHM PHARMA INC., NDC labeler code 66096. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Acne Relief Gel?: 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.