What is NDC 62795-1016?

62795-1016 is the product NDC for BHI Skin, Berberis vulgaris root bark 6 [hp_X]/1 + 7 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

BHI Skin (BERBERIS VULGARIS ROOT BARK, GRAPHITE, HYDROFLUORIC ACID, LYCOPODIUM CLAVATUM SPORE, PETROLATUM, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, and SULFUR).

What is the active ingredient?

Berberis vulgaris root bark, Graphite, Hydrofluoric acid, Lycopodium clavatum spore, Petrolatum, Toxicodendron pubescens leaf, Sepia officinalis juice, Sulfur.

MediNatura Inc, NDC labeler code 62795. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for BHI Skin?

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.

BHI Skin NDC 62795-1016 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1016Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1016Add 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
62795-1016-3	6279510160362795101603	1 PACKAGE in 1 CARTON (62795-1016-3) / 100 TABLET in 1 PACKAGEMarketed from Jan 1, 2015

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): BHI Skin
Generic name (nonproprietary): berberis vulgaris root bark, graphite, hydrofluoric acid, lycopodium clavatum spore, petrolatum, toxicodendron pubescens leaf, sepia officinalis juice, and sulfur
Active ingredients: Berberis vulgaris root bark — 6 [hp_X]/1Graphite — 10 [hp_X]/1Hydrofluoric acid — 10 [hp_X]/1Lycopodium clavatum spore — 12 [hp_X]/1Petrolatum — 10 [hp_X]/1Toxicodendron pubescens leaf — 8 [hp_X]/1Sepia officinalis juice — 10 [hp_X]/1Sulfur — 12 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: MediNatura IncNDC labeler code 62795
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Jan 1, 2015
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-1016_29e7a2ad-a3bb-4527-a81d-0c6b4dba65a5SPL ID 29e7a2ad-a3bb-4527-a81d-0c6b4dba65a5SPL set ID 70ab2931-bd2d-43de-bb36-d019f78e3d73UNII 1TH8Q20J0U, 4QQN74LH4O, RGL5YE86CZ, C88X29Y479, 4T6H12BN9U, 6IO182RP7A, QDL83WN8C2, 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

N462795101603 followed by a unit qualifier and the quantity

Package 62795-1016-03. 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 Jul 7, 2022.

Indications (excerpt from the label)

USES For the temporary relief of minor eczema symptoms: rough scaly skin, itching skin, redness

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62795-1016

What is NDC 62795-1016?: 62795-1016 is the product NDC for BHI Skin, Berberis vulgaris root bark 6 [hp_X]/1 + 7 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: BHI Skin (BERBERIS VULGARIS ROOT BARK, GRAPHITE, HYDROFLUORIC ACID, LYCOPODIUM CLAVATUM SPORE, PETROLATUM, TOXICODENDRON PUBESCENS LEAF, SEPIA OFFICINALIS JUICE, and SULFUR).
What is the active ingredient?: Berberis vulgaris root bark, Graphite, Hydrofluoric acid, Lycopodium clavatum spore, Petrolatum, Toxicodendron pubescens leaf, Sepia officinalis juice, Sulfur.
Who is the labeler?: MediNatura Inc, NDC labeler code 62795. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for BHI Skin?: 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.