lidopro pain relief

Generic: capsaicin and lidocaine

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name lidopro pain relief
Generic Name capsaicin and lidocaine
Labeler preferred pharmaceuticals inc.
Dosage Form OINTMENT
Routes
TRANSDERMAL
Active Ingredients

capsaicin .0325 mg/100mg, lidocaine hydrochloride 4 mg/100mg, menthol, (+)- 10 mg/100mg, methyl salicylate 27.5 mg/100mg

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-8833
Product ID 68788-8833_c259ef92-5d07-4590-adf1-3a106333eee0
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2025-02-21

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 687888833
Hyphenated Format 68788-8833

Supplemental Identifiers

RxCUI
1601095 1601097
UNII
S07O44R1ZM V13007Z41A C6B1OE8P3W LAV5U5022Y

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name lidopro pain relief (source: ndc)
Generic Name capsaicin and lidocaine (source: ndc)
Application Number M017 (source: ndc)
Routes
TRANSDERMAL
source: ndc

Resolved Composition

Strengths
  • .0325 mg/100mg
  • 4 mg/100mg
  • 10 mg/100mg
  • 27.5 mg/100mg
source: ndc
Packaging
  • 1 TUBE, WITH APPLICATOR in 1 BOX (68788-8833-9) / 9900 mg in 1 TUBE, WITH APPLICATOR
source: ndc

Packages (1)

68788-8833-9 1 TUBE, WITH APPLICATOR in 1 BOX (68788-8833-9) / 9900 mg in 1 TUBE, WITH APPLICATOR

Ingredients (4)

capsaicin (.0325 mg/100mg) lidocaine hydrochloride (4 mg/100mg) menthol, (+)- (10 mg/100mg) methyl salicylate (27.5 mg/100mg)

Linked Drug Pages (1)

LidoPro Pain Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TRANSDERMAL"], "spl_id": "c259ef92-5d07-4590-adf1-3a106333eee0", "openfda": {"unii": ["S07O44R1ZM", "V13007Z41A", "C6B1OE8P3W", "LAV5U5022Y"], "rxcui": ["1601095", "1601097"], "spl_set_id": ["c259ef92-5d07-4590-adf1-3a106333eee0"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 BOX (68788-8833-9)  / 9900 mg in 1 TUBE, WITH APPLICATOR", "package_ndc": "68788-8833-9", "marketing_start_date": "20250221"}], "brand_name": "LidoPro Pain Relief", "product_id": "68788-8833_c259ef92-5d07-4590-adf1-3a106333eee0", "dosage_form": "OINTMENT", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "68788-8833", "generic_name": "Capsaicin and Lidocaine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LidoPro Pain Relief", "active_ingredients": [{"name": "CAPSAICIN", "strength": ".0325 mg/100mg"}, {"name": "LIDOCAINE HYDROCHLORIDE", "strength": "4 mg/100mg"}, {"name": "MENTHOL, (+)-", "strength": "10 mg/100mg"}, {"name": "METHYL SALICYLATE", "strength": "27.5 mg/100mg"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250221", "listing_expiration_date": "20261231"}