What is NDC 70163-0022?

70163-0022 is the product NDC for Pain Relief, Arnica montana whole 6 [hp_X]/1 + 6 more ingredients tablet, listed with the FDA by NaturalCare. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Pain Relief (Arnica Montana, Belladonna, Gelsemium Sempervirens, Gnaphalium Polycephalum, Magnesia Phosphorica, Sanguinaria Canadensis, Salix Alba).

What is the active ingredient?

Arnica montana whole, Atropa belladonna, Gelsemium sempervirens root, Pseudognaphalium obtusifolium whole, Magnesium phosphate, Dibasic trihydrate, Sanguinaria canadensis root, Salix alba bark.

NaturalCare, NDC labeler code 70163. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Pain Relief?

62 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Pain Relief NDC 70163-0022 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70163-0022Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70163-0022Add 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
70163-0022-1	7016300220170163002201	1 BLISTER PACK in 1 CARTON (70163-0022-1) / 60 TABLET in 1 BLISTER PACKMarketed from Mar 2, 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): Pain Relief
Generic name (nonproprietary): arnica montana, belladonna, gelsemium sempervirens, gnaphalium polycephalum, magnesia phosphorica, sanguinaria canadensis, salix alba
Active ingredients: Arnica montana whole — 6 [hp_X]/1Atropa belladonna — 6 [hp_X]/1Gelsemium sempervirens root — 6 [hp_X]/1Pseudognaphalium obtusifolium whole — 6 [hp_X]/1Magnesium phosphate, Dibasic trihydrate — 6 [hp_X]/1Sanguinaria canadensis root — 6 [hp_X]/1Salix alba bark — 4 [hp_X]/1
Dosage form: Tablet
Route: Oral
Labeler: NaturalCareNDC labeler code 70163
Product type: Over-the-counter drug
Marketing category: Unapproved homeopathic
Marketing start: Mar 2, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Small Intestine Fluid/Electrolyte Absorption (Physiologic effect)Magnesium Ion Exchange Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 70163-0022_29da8ff5-dada-4222-937b-b2d2c6ad1c44SPL ID 29da8ff5-dada-4222-937b-b2d2c6ad1c44SPL set ID 6eba2caa-958f-47a1-823c-c73bbb1d7fa9UNII O80TY208ZW, WQZ3G9PF0H, 639KR60Q1Q, 36XQ854NWW, HF539G9L3Q, N9288CD508, 205MXS71H7
Pharmacologic class: Calculi Dissolution Agent; Osmotic Laxative

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

N470163002201 followed by a unit qualifier and the quantity

Package 70163-0022-01. 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 2, 2026.

Indications (excerpt from the label)

USES: May help temporarily relieve ■ back pain ■ headaches ■ leg cramps ■ muscle pain ■ sciatica pain* *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)

About NDC 70163-0022

What is NDC 70163-0022?: 70163-0022 is the product NDC for Pain Relief, Arnica montana whole 6 [hp_X]/1 + 6 more ingredients tablet, listed with the FDA by NaturalCare. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Pain Relief (Arnica Montana, Belladonna, Gelsemium Sempervirens, Gnaphalium Polycephalum, Magnesia Phosphorica, Sanguinaria Canadensis, Salix Alba).
What is the active ingredient?: Arnica montana whole, Atropa belladonna, Gelsemium sempervirens root, Pseudognaphalium obtusifolium whole, Magnesium phosphate, Dibasic trihydrate, Sanguinaria canadensis root, Salix alba bark.
Who is the labeler?: NaturalCare, NDC labeler code 70163. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Pain Relief?: 62 other product NDCs are listed under this name. See all Pain Relief NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Pain Relief NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Pain Reliefacetaminophen	Acetaminophen 325 mg/1	TabletOral	Shield Pharmaceuticals Corp.	83059-0160	—
Pain Reliefmenthol spray	Menthol 76.6 mg/mL	SprayTopical	Owell Naturals Brand, LLC	83570-003	83570-0003-02
pain reliefacetaminophen	Acetaminophen 500 mg/1	Tablet, Film coatedOral	HyVee Inc	42507-813	42507-0813-78
Pain Reliefmenthol	Menthol 10.5 g/100mL	SprayTopical	Trifecta Pharmaceuticals USA, LLC.	69396-175	69396-0175-03
Pain Reliefacetaminophen	Acetaminophen 500 mg/1	TabletOral	HYVEE INC	42507-103	42507-0103-04
Pain Reliefacetaminophen	Acetaminophen 650 mg/1	Tablet, Extended releaseOral	HYVEE INC	42507-303	42507-0303-03
Pain Reliefacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	HYVEE INC	42507-404	42507-0404-09
Pain Reliefacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	HYVEE INC	42507-592	42507-0592-03
Pain Relieflidocaine	Lidocaine .04 g/g	PatchTopical	Shanghai Chuangshi Medical Technology (Group) Co., Ltd.	73557-189	73557-0189-30
Pain Reliefacetaminophen	Acetaminophen 500 mg/1	Tablet, CoatedOral	HYVEE INC	42507-170	42507-0170-0142507-0170-0242507-0170-03+1 more

All 63 Pain Relief NDCs