bluestop max

Generic: external analgesic

Labeler: clavel corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name bluestop max
Generic Name external analgesic
Labeler clavel corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

lidocaine hydrochloride 40 mg/g, menthol 10 mg/g

Manufacturer
Clavel Corporation

Identifiers & Regulatory

Product NDC 82714-001
Product ID 82714-001_4835cc39-0fd2-f27e-e063-6294a90abf4f
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M017
Listing Expiration 2027-12-31
Marketing Start 2023-01-10

Pharmacologic Class

Classes
amide local anesthetic [epc] amides [cs] antiarrhythmic [epc] local anesthesia [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 82714001
Hyphenated Format 82714-001

Supplemental Identifiers

RxCUI
1373137
UPC
0832492046835
UNII
V13007Z41A 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 bluestop max (source: ndc)
Generic Name external analgesic (source: ndc)
Application Number M017 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 40 mg/g
  • 10 mg/g
source: ndc
Packaging
  • 1 APPLICATOR in 1 CARTON (82714-001-01) / 85 g in 1 APPLICATOR
source: ndc

Packages (1)

82714-001-01 1 APPLICATOR in 1 CARTON (82714-001-01) / 85 g in 1 APPLICATOR

Ingredients (2)

lidocaine hydrochloride (40 mg/g) menthol (10 mg/g)

Linked Drug Pages (1)

BlueStop Max ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4835cc39-0fd2-f27e-e063-6294a90abf4f", "openfda": {"upc": ["0832492046835"], "unii": ["V13007Z41A", "L7T10EIP3A"], "rxcui": ["1373137"], "spl_set_id": ["f1efb51c-5217-4cb2-e053-2a95a90a7f95"], "manufacturer_name": ["Clavel Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 APPLICATOR in 1 CARTON (82714-001-01)  / 85 g in 1 APPLICATOR", "package_ndc": "82714-001-01", "marketing_start_date": "20230110"}], "brand_name": "BlueStop Max", "product_id": "82714-001_4835cc39-0fd2-f27e-e063-6294a90abf4f", "dosage_form": "GEL", "pharm_class": ["Amide Local Anesthetic [EPC]", "Amides [CS]", "Antiarrhythmic [EPC]", "Local Anesthesia [PE]"], "product_ndc": "82714-001", "generic_name": "External Analgesic", "labeler_name": "Clavel Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "BlueStop Max", "active_ingredients": [{"name": "LIDOCAINE HYDROCHLORIDE", "strength": "40 mg/g"}, {"name": "MENTHOL", "strength": "10 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230110", "listing_expiration_date": "20271231"}