FDA.reportPublic FDA data

Hemorrhoid Cream

Product NDC
85056-003
11-digit product format
850560003
Labeler code
85056
Product ID
85056-003_426ce6a2-80a2-0260-e063-6294a90ace17
Type
HUMAN OTC DRUG
Nonproprietary name
Hemorrhoid Cream
Dosage form
CREAM
Route
CUTANEOUS
Labeler
Henan Shouerkang Health Industry Co., Ltd
Application
505G(a)(3)
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2025-10-31
Substance
.ALPHA.-TOCOPHEROL; ALOE; WITCH HAZEL; ZINC OXIDE
Active strength
1; 1; 3; 10 g/100g; g/100g; g/100g; g/100g
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
.ALPHA.-TOCOPHEROL1 g/100g
ALOE1 g/100g
WITCH HAZEL3 g/100g
ZINC OXIDE10 g/100g

Harmonized Identifiers#

Field, Values table
FieldValues
UniiH4N855PNZ1, V5VD430YW9, 101I4J0U34, SOI2LOH54Z

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85056-003-01Hemorrhoid Cream10 g in 1 TUBECREAM101
85056-003-02Hemorrhoid Cream15 g in 1 TUBECREAM151
85056-003-03Hemorrhoid Cream20 g in 1 TUBECREAM201
85056-003-04Hemorrhoid Cream28 g in 1 TUBECREAM281
85056-003-05Hemorrhoid Cream57 g in 1 TUBECREAM571

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
85056-003-018505600030110 g in 1 TUBE (85056-003-01) 10 g2025-10-31NoNoCurrent
85056-003-028505600030215 g in 1 TUBE (85056-003-02) 15 g2025-10-31NoNoCurrent
85056-003-038505600030320 g in 1 TUBE (85056-003-03) 20 g2025-10-31NoNoCurrent
85056-003-048505600030428 g in 1 TUBE (85056-003-04) 28 g2025-10-31NoNoCurrent
85056-003-058505600030557 g in 1 TUBE (85056-003-05) 57 g2025-10-31NoNoCurrent