What is NDC 62795-1007?

62795-1007 is the product NDC for BHI Back, Ammonium chloride 6 [hp_X]/1 + 5 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

BHI Back (AMMONIUM CHLORIDE, MATRICARIA RECUTITA,CITRULLUS COLOCYNTHIS FRUIT PULP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, and TOXICODENDRON PUBESCENS LEAF).

What is the active ingredient?

Ammonium chloride, Matricaria recutita, Citrullus colocynthis fruit pulp, Gelsemium sempervirens root, Pseudognaphalium obtusifolium, Toxicodendron pubescens leaf.

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 Back?

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 Back NDC 62795-1007 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62795-1007Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62795-1007Add 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
62795-1007-2	6279510070262795100702	100 TABLET in 1 BOTTLE (62795-1007-2)Marketed from May 23, 2023
62795-1007-3	6279510070362795100703	1 BOTTLE in 1 CARTON (62795-1007-3) / 100 TABLET in 1 BOTTLEMarketed from Aug 30, 2014

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 Back
Generic name (nonproprietary): ammonium chloride, matricaria recutita,citrullus colocynthis fruit pulp, pseudognaphalium obtusifolium, and toxicodendron pubescens leaf
Active ingredients: Ammonium chloride — 6 [hp_X]/1Matricaria recutita — 10 [hp_X]/1Citrullus colocynthis fruit pulp — 5 [hp_X]/1Gelsemium sempervirens root — 6 [hp_X]/1Pseudognaphalium obtusifolium — 5 [hp_X]/1Toxicodendron pubescens leaf — 8 [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: Aug 30, 2014
Listing expires: Dec 31, 2026
Identifiers: Product ID 62795-1007_af2b8787-5aee-4b15-afe6-65f1beaa0201SPL ID af2b8787-5aee-4b15-afe6-65f1beaa0201SPL set ID aa622a5b-16de-4098-9c3f-d7569f7d2c2fUNII 01Q9PC255D, G0R4UBI2ZZ, 23H32AOH17, 639KR60Q1Q, 36XQ854NWW, 6IO182RP7A

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

N462795100702 followed by a unit qualifier and the quantity

Package 62795-1007-02. 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 23, 2023.

Indications (excerpt from the label)

USES For the temporary relief of minor back pain, leg & hip pain, muscle spasm

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62795-1007

What is NDC 62795-1007?: 62795-1007 is the product NDC for BHI Back, Ammonium chloride 6 [hp_X]/1 + 5 more ingredients tablet, listed with the FDA by MediNatura Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: BHI Back (AMMONIUM CHLORIDE, MATRICARIA RECUTITA,CITRULLUS COLOCYNTHIS FRUIT PULP, PSEUDOGNAPHALIUM OBTUSIFOLIUM, and TOXICODENDRON PUBESCENS LEAF).
What is the active ingredient?: Ammonium chloride, Matricaria recutita, Citrullus colocynthis fruit pulp, Gelsemium sempervirens root, Pseudognaphalium obtusifolium, Toxicodendron pubescens leaf.
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 Back?: 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.