xcellderma
Generic: wound cream
Labeler: regenerex pharma incDrug Facts
Product Profile
Brand Name
xcellderma
Generic Name
wound cream
Labeler
regenerex pharma inc
Dosage Form
CREAM
Routes
Active Ingredients
zinc acetate .001 g/g
Manufacturer
Identifiers & Regulatory
Product NDC
84076-111
Product ID
84076-111_351c4e48-bfe9-1023-e063-6394a90ac6e7
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M016
Listing Expiration
2026-12-31
Marketing Start
2024-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84076111
Hyphenated Format
84076-111
Supplemental Identifiers
UNII
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
xcellderma (source: ndc)
Generic Name
wound cream (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .001 g/g
Packaging
- 30 g in 1 TUBE (84076-111-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "351c4e48-bfe9-1023-e063-6394a90ac6e7", "openfda": {"unii": ["FM5526K07A"], "spl_set_id": ["116e2c97-2210-eb46-e063-6294a90a5454"], "manufacturer_name": ["Regenerex Pharma INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 g in 1 TUBE (84076-111-01)", "package_ndc": "84076-111-01", "marketing_start_date": "20240301"}], "brand_name": "Xcellderma", "product_id": "84076-111_351c4e48-bfe9-1023-e063-6394a90ac6e7", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]"], "product_ndc": "84076-111", "generic_name": "Wound Cream", "labeler_name": "Regenerex Pharma INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Xcellderma", "active_ingredients": [{"name": "ZINC ACETATE", "strength": ".001 g/g"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}