ultra-strength pain relief analgesic
Generic: camphor (synthetic) and menthol, unspecified form
Labeler: target corporationDrug Facts
Product Profile
Brand Name
ultra-strength pain relief analgesic
Generic Name
camphor (synthetic) and menthol, unspecified form
Labeler
target corporation
Dosage Form
OINTMENT
Routes
Active Ingredients
camphor (synthetic) 110 mg/g, menthol, unspecified form 110 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
82442-311
Product ID
82442-311_9029fd41-a09a-4651-828c-5b033dd14c9a
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2026-12-31
Marketing Start
2024-10-14
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
82442311
Hyphenated Format
82442-311
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ultra-strength pain relief analgesic (source: ndc)
Generic Name
camphor (synthetic) and menthol, unspecified form (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 110 mg/g
Packaging
- 1 JAR in 1 CARTON (82442-311-01) / 18 g in 1 JAR
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "9029fd41-a09a-4651-828c-5b033dd14c9a", "openfda": {"unii": ["5TJD82A1ET", "L7T10EIP3A"], "rxcui": ["1089847"], "spl_set_id": ["159c5a84-bf68-41dd-a2d3-bc2402037244"], "manufacturer_name": ["TARGET CORPORATION"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 JAR in 1 CARTON (82442-311-01) / 18 g in 1 JAR", "package_ndc": "82442-311-01", "marketing_start_date": "20241014"}], "brand_name": "Ultra-Strength Pain Relief Analgesic", "product_id": "82442-311_9029fd41-a09a-4651-828c-5b033dd14c9a", "dosage_form": "OINTMENT", "product_ndc": "82442-311", "generic_name": "CAMPHOR (SYNTHETIC) and MENTHOL, UNSPECIFIED FORM", "labeler_name": "TARGET CORPORATION", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ultra-Strength Pain Relief", "brand_name_suffix": "Analgesic", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "110 mg/g"}, {"name": "MENTHOL, UNSPECIFIED FORM", "strength": "110 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20241014", "listing_expiration_date": "20261231"}