Gout

Product NDC
82877-001
11-digit product format
828770001
Labeler code
82877
Product ID
82877-001_e32f72db-5ce8-36a7-e053-2a95a90abbfa
Type
HUMAN OTC DRUG
Nonproprietary name
Gout Ointment
Dosage form
OINTMENT
Route
CUTANEOUS
Labeler
Shenzhen Boceda New Technology Co., Ltd.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-07-07
Marketing end
0000-00-00
Substance
CHLORHEXIDINE ACETATE
Active strength
0 g/100g
Pharmacologic classes
Decreased Cell Wall Integrity [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
bb6d6c68-649d-4e6d-a1f6-603d969c8f68Product name120160303

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
82877-001-01Gout20 g in 1 BOXOINTMENT201
82877-001-02Gout30 g in 1 BOXOINTMENT301
82877-001-03Gout50 g in 1 BOXOINTMENT501
82877-001-04Gout100 g in 1 BOXOINTMENT1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
82877-001GOUT (GOUT OINTMENT) OINTMENT [SHENZHEN BOCEDA NEW TECHNOLOGY CO., LTD.]1Legacy NDC, 4 package rows20220713_e32f72db-5ce7-36a7-e053-2a95a90abbfa.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
82877-001-018287700010120 g in 1 BOX (82877-001-01) 20 g2022-07-070000-00-00NoNoCurrent
82877-001-028287700010230 g in 1 BOX (82877-001-02) 30 g2022-07-070000-00-00NoNoCurrent
82877-001-038287700010350 g in 1 BOX (82877-001-03) 50 g2022-07-070000-00-00NoNoCurrent
82877-001-0482877000104100 g in 1 BOX (82877-001-04) 100 g2022-07-070000-00-00NoNoCurrent