doctor hoys pain relief gel

Generic: menthol, camphor (synthetic)

Labeler: dynamic blending specialists, inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name doctor hoys pain relief gel
Generic Name menthol, camphor (synthetic)
Labeler dynamic blending specialists, inc.
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

camphor (synthetic) 50 mg/mL, menthol 50 mg/mL

Manufacturer
Dynamic Blending Specialists, Inc.

Identifiers & Regulatory

Product NDC 75638-010
Product ID 75638-010_4769df6d-225f-5a0d-e063-6394a90af652
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Marketing Start 2023-03-01
Marketing End 2028-04-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 75638010
Hyphenated Format 75638-010

Supplemental Identifiers

RxCUI
797500
UNII
5TJD82A1ET 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 doctor hoys pain relief gel (source: ndc)
Generic Name menthol, camphor (synthetic) (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/mL
source: ndc
Packaging
  • 89 mL in 1 TUBE (75638-010-00)
  • 177 mL in 1 TUBE (75638-010-01)
  • 946 mL in 1 TUBE (75638-010-02)
  • 1893 mL in 1 TUBE (75638-010-03)
source: ndc

Packages (4)

Ingredients (2)

camphor (synthetic) (50 mg/mL) menthol (50 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4769df6d-225f-5a0d-e063-6394a90af652", "openfda": {"unii": ["5TJD82A1ET", "L7T10EIP3A"], "rxcui": ["797500"], "spl_set_id": ["50123bb9-d5d8-4ba6-ab94-8ed95fe0f5a8"], "manufacturer_name": ["Dynamic Blending Specialists, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "89 mL in 1 TUBE (75638-010-00)", "package_ndc": "75638-010-00", "marketing_end_date": "20280413", "marketing_start_date": "20230301"}, {"sample": false, "description": "177 mL in 1 TUBE (75638-010-01)", "package_ndc": "75638-010-01", "marketing_end_date": "20280124", "marketing_start_date": "20230301"}, {"sample": false, "description": "946 mL in 1 TUBE (75638-010-02)", "package_ndc": "75638-010-02", "marketing_end_date": "20280124", "marketing_start_date": "20230301"}, {"sample": false, "description": "1893 mL in 1 TUBE (75638-010-03)", "package_ndc": "75638-010-03", "marketing_end_date": "20280124", "marketing_start_date": "20230301"}], "brand_name": "Doctor Hoys Pain Relief Gel", "product_id": "75638-010_4769df6d-225f-5a0d-e063-6394a90af652", "dosage_form": "GEL", "product_ndc": "75638-010", "generic_name": "MENTHOL, CAMPHOR (SYNTHETIC)", "labeler_name": "Dynamic Blending Specialists, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Doctor Hoys Pain Relief Gel", "active_ingredients": [{"name": "CAMPHOR (SYNTHETIC)", "strength": "50 mg/mL"}, {"name": "MENTHOL", "strength": "50 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_end_date": "20280413", "marketing_start_date": "20230301"}