Unguentine

Product NDC
45728-446
11-digit product format
457280446
Labeler code
45728
Product ID
45728-446_327038a1-b826-1199-e063-6394a90a7f5f
Type
HUMAN OTC DRUG
Nonproprietary name
phenol, zinc oxide
Dosage form
OINTMENT
Route
TOPICAL
Labeler
Oakhurst Company
Application
M003
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-04-10
Substance
PHENOL; ZINC OXIDE
Active strength
.015; .066 g/g; g/g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Unguentine
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
PHENOL.015 g/g
ZINC OXIDE.066 g/g

Harmonized Identifiers#

Field, Values table
FieldValues
Unii339NCG44TV, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
45728-446-99Unguentine1 in 1 CARTONOINTMENT11
45728-446-99Unguentine28 g in 1 TUBEOINTMENT281

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
45728-446UNGUENTINE (PHENOL, ZINC OXIDE) OINTMENT [OAKHURST COMPANY]1Current NDC, 2 package rows20250413_327038a1-b825-1199-e063-6394a90a7f5f.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
45728-446-99457280446991 TUBE in 1 CARTON (45728-446-99) / 28 g in 1 TUBE1 tube2025-04-10NoNoCurrent