DRMITSUI FOOT ANTIFUNGAL TREATMENT

Product NDC
87096-004
11-digit product format
870960004
Labeler code
87096
Product ID
87096-004_4ce59d31-56ff-d74f-e063-6294a90a7cce
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic acid
Dosage form
SPRAY
Route
PERCUTANEOUS
Labeler
Zhenping Renren Industry Co., Ltd.
Application
M005
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2026-03-14
Substance
SALICYLIC ACID
Active strength
12 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
DRMITSUI FOOT ANTIFUNGAL TREATMENT
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID12 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiO414PZ4LPZ
Rxcui2738916

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87096-004-01DRMITSUI FOOT ANTIFUNGAL TREATMENT60 g in 1 BOTTLE, SPRAYSPRAY601

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2738916salicylic acid 12 % Topical SprayPSN4ce59d31-56fe-d74f-e063-6294a90a7cce1
2738916salicylic acid 120 MG/ML Topical SpraySCD4ce59d31-56fe-d74f-e063-6294a90a7cce1
2738916salicylic acid 12 % Topical SpraySY4ce59d31-56fe-d74f-e063-6294a90a7cce1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
87096-004-018709600040160 g in 1 BOTTLE, SPRAY (87096-004-01) 60 g2026-03-14NoNoHistorical