orca complete menthol pain reliever

Generic: menthol

Labeler: orca products, llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name orca complete menthol pain reliever
Generic Name menthol
Labeler orca products, llc
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

menthol, unspecified form 20 mg/mL

Manufacturer
ORCA Products, LLC

Identifiers & Regulatory

Product NDC 82939-000
Product ID 82939-000_0c06e3d2-4481-f4b5-e063-6394a90a0608
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M022
Listing Expiration 2026-12-31
Marketing Start 2022-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82939000
Hyphenated Format 82939-000

Supplemental Identifiers

RxCUI
2611702
UPC
0860003109939
UNII
L7T10EIP3A

Packaging Origin

Original Packager
true

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 orca complete menthol pain reliever (source: ndc)
Generic Name menthol (source: ndc)
Application Number M022 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 BOX (82939-000-02) / 13 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

menthol, unspecified form (20 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c06e3d2-4481-f4b5-e063-6394a90a0608", "openfda": {"upc": ["0860003109939"], "unii": ["L7T10EIP3A"], "rxcui": ["2611702"], "spl_set_id": ["99990e27-d66b-4d61-97f2-6a76066eb8b8"], "manufacturer_name": ["ORCA Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (82939-000-02)  / 13 mL in 1 BOTTLE", "package_ndc": "82939-000-02", "marketing_start_date": "20230915"}], "brand_name": "ORCA Complete Menthol Pain Reliever", "product_id": "82939-000_0c06e3d2-4481-f4b5-e063-6394a90a0608", "dosage_form": "LIQUID", "product_ndc": "82939-000", "generic_name": "MENTHOL", "labeler_name": "ORCA Products, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ORCA Complete Menthol Pain Reliever", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "20 mg/mL"}], "application_number": "M022", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220915", "listing_expiration_date": "20261231"}