super white stuff pain relief

Generic: menthol

Labeler: blue spring wellness, l.l.c.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name super white stuff pain relief
Generic Name menthol
Labeler blue spring wellness, l.l.c.
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

menthol 14 mg/mL

Manufacturer
BLUE SPRING WELLNESS, L.L.C.

Identifiers & Regulatory

Product NDC 14448-302
Product ID 14448-302_09d7052e-ec40-ef60-e063-6294a90af214
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2026-12-31
Marketing Start 2020-08-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14448302
Hyphenated Format 14448-302

Supplemental Identifiers

RxCUI
2391332
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 super white stuff pain relief (source: ndc)
Generic Name menthol (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 14 mg/mL
source: ndc
Packaging
  • 85 mL in 1 BOTTLE (14448-302-30)
source: ndc

Packages (1)

Ingredients (1)

menthol (14 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "09d7052e-ec40-ef60-e063-6294a90af214", "openfda": {"unii": ["L7T10EIP3A"], "rxcui": ["2391332"], "spl_set_id": ["1231ddd2-7661-45b2-ab15-32f7fdc078a8"], "manufacturer_name": ["BLUE SPRING WELLNESS, L.L.C."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 mL in 1 BOTTLE (14448-302-30)", "package_ndc": "14448-302-30", "marketing_start_date": "20200801"}], "brand_name": "SUPER WHITE STUFF Pain Relief", "product_id": "14448-302_09d7052e-ec40-ef60-e063-6294a90af214", "dosage_form": "CREAM", "product_ndc": "14448-302", "generic_name": "MENTHOL", "labeler_name": "BLUE SPRING WELLNESS, L.L.C.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "SUPER WHITE STUFF Pain Relief", "active_ingredients": [{"name": "MENTHOL", "strength": "14 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200801", "listing_expiration_date": "20261231"}