pain relieving gel
Generic: menthol
Labeler: rite aid corporationDrug Facts
Product Profile
Brand Name
pain relieving gel
Generic Name
menthol
Labeler
rite aid corporation
Dosage Form
GEL
Routes
Active Ingredients
menthol, unspecified form 40 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11822-8940
Product ID
11822-8940_49a14713-5b28-9721-e063-6294a90a8401
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M017
Listing Expiration
2027-12-31
Marketing Start
2023-02-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
118228940
Hyphenated Format
11822-8940
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
pain relieving gel (source: ndc)
Generic Name
menthol (source: ndc)
Application Number
M017 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 40 mg/mL
Packaging
- 74 mL in 1 BOTTLE, WITH APPLICATOR (11822-8940-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "49a14713-5b28-9721-e063-6294a90a8401", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["415974"], "spl_set_id": ["10e3ad07-0d41-7b15-e063-6294a90a0407"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE, WITH APPLICATOR (11822-8940-1)", "package_ndc": "11822-8940-1", "marketing_start_date": "20230201"}], "brand_name": "Pain Relieving Gel", "product_id": "11822-8940_49a14713-5b28-9721-e063-6294a90a8401", "dosage_form": "GEL", "product_ndc": "11822-8940", "generic_name": "Menthol", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Pain Relieving Gel", "active_ingredients": [{"name": "MENTHOL, UNSPECIFIED FORM", "strength": "40 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230201", "listing_expiration_date": "20271231"}