wowday hemorrhoid and fissure cream
Generic: hemorrhoid and fissure cream
Labeler: wowday llcDrug Facts
Product Profile
Brand Name
wowday hemorrhoid and fissure cream
Generic Name
hemorrhoid and fissure cream
Labeler
wowday llc
Dosage Form
CREAM
Routes
Active Ingredients
glycerin 3 g/15g, menthol .075 g/15g, witch hazel 3.75 g/15g
Manufacturer
Identifiers & Regulatory
Product NDC
87113-1008
Product ID
87113-1008_4aa59584-e9b1-1f3f-e063-6394a90aeb21
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M015
Listing Expiration
2027-12-31
Marketing Start
2026-02-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
871131008
Hyphenated Format
87113-1008
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
wowday hemorrhoid and fissure cream (source: ndc)
Generic Name
hemorrhoid and fissure cream (source: ndc)
Application Number
M015 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 g/15g
- .075 g/15g
- 3.75 g/15g
Packaging
- 1 TUBE, WITH APPLICATOR in 1 BOX (87113-1008-1) / 2 g in 1 TUBE, WITH APPLICATOR
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RECTAL"], "spl_id": "4aa59584-e9b1-1f3f-e063-6394a90aeb21", "openfda": {"nui": ["N0000185370", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0009417"], "unii": ["PDC6A3C0OX", "L7T10EIP3A", "101I4J0U34"], "rxcui": ["2734148"], "spl_set_id": ["47ba86ad-240a-e733-e063-6394a90a24e3"], "pharm_class_cs": ["Allergens [CS]", "Glycerol [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Non-Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["WowDay LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE, WITH APPLICATOR in 1 BOX (87113-1008-1) / 2 g in 1 TUBE, WITH APPLICATOR", "package_ndc": "87113-1008-1", "marketing_start_date": "20260201"}], "brand_name": "WowDay Hemorrhoid and Fissure Cream", "product_id": "87113-1008_4aa59584-e9b1-1f3f-e063-6394a90aeb21", "dosage_form": "CREAM", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Glycerol [CS]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Non-Standardized Chemical Allergen [EPC]"], "product_ndc": "87113-1008", "generic_name": "Hemorrhoid and Fissure Cream", "labeler_name": "WowDay LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "WowDay Hemorrhoid and Fissure Cream", "active_ingredients": [{"name": "GLYCERIN", "strength": "3 g/15g"}, {"name": "MENTHOL", "strength": ".075 g/15g"}, {"name": "WITCH HAZEL", "strength": "3.75 g/15g"}], "application_number": "M015", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20260201", "listing_expiration_date": "20271231"}