Sumifun Knee Relieve Patch

Product NDC
83781-007
11-digit product format
837810007
Labeler code
83781
Product ID
83781-007_0e031aa5-edf5-8c9d-e063-6394a90afee3
Type
HUMAN OTC DRUG
Nonproprietary name
Knee Relieve Patch
Dosage form
PATCH
Route
TOPICAL
Labeler
Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd
Application
M017
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-01-02
Substance
BORNEOL; CAMPHOR (SYNTHETIC); MENTHOL
Active strength
1.2; 1.5; 1 g/1001; g/1001; g/1001
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Sumifun Knee Relieve Patch
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BORNEOL1.2 g/1001
CAMPHOR (SYNTHETIC)1.5 g/1001
MENTHOL1 g/1001

Harmonized Identifiers#

Field, Values table
FieldValues
UniiM89NIB437X, 5TJD82A1ET, L7T10EIP3A

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83781-007-01Sumifun Knee Relieve Patch24 in 1 BOXPATCH241

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83781-007SUMIFUN KNEE RELIEVE PATCH (KNEE RELIEVE PATCH) PATCH [ZHENGZHOU MIAOQI PHARMACEUTICAL TECHNOLOGY CO., LTD]1Current NDC, 1 package rows20240103_0e031aa5-edf4-8c9d-e063-6394a90afee3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83781-007-018378100070124 PATCH in 1 BOX (83781-007-01) 24 patch2024-01-02NoNoCurrent