Remaxazon External Patch

FDA-approved pharmaceutical product with comprehensive regulatory information, manufacturing details, and complete labeling documentation.

Company

DUNS: 783518983

Effective Date

March 9, 2015

Labeling Type

HUMAN PRESCRIPTION DRUG LABEL

Active Ingredients

chondroitin sulfate sodium (bovine)(3 g in 100 g)

Glucosamine(5 g in 100 g)

Capsaicin(.0285 g in 100 g)

Lidocaine(4 g in 100 g)

Products1

Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.

NDC Product Code

69379-285

Route of Administration

TOPICAL

Effective Date

March 9, 2015

Ingredients

chondroitin sulfate sodium (bovine)Active

Code: 8QTV3DTT8WClass: ACTIMQuantity: 3 g in 100 g

Code: N08U5BOQ1KClass: ACTIBQuantity: 5 g in 100 g

Code: S07O44R1ZMClass: ACTIBQuantity: .0285 g in 100 g

Code: 98PI200987Class: ACTIBQuantity: 4 g in 100 g