anubismed
Generic: sodium bicarbonate, aloe barbadensis leaf juice, imidazolidinyl urea
Labeler: anubis cosmetics slDrug Facts
Product Profile
Brand Name
anubismed
Generic Name
sodium bicarbonate, aloe barbadensis leaf juice, imidazolidinyl urea
Labeler
anubis cosmetics sl
Dosage Form
LIQUID
Routes
Active Ingredients
aloe vera leaf .15 g/50mL, imidurea .25 g/50mL, water 45.8293 mL/50mL
Manufacturer
Identifiers & Regulatory
Product NDC
83021-400
Product ID
83021-400_049fe4c2-996a-198f-e063-6294a90a40b9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH FINAL
Application Number
M016
Marketing Start
2022-10-26
Marketing End
2027-05-10
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
83021400
Hyphenated Format
83021-400
Supplemental Identifiers
UPC
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
anubismed (source: ndc)
Generic Name
sodium bicarbonate, aloe barbadensis leaf juice, imidazolidinyl urea (source: ndc)
Application Number
M016 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .15 g/50mL
- .25 g/50mL
- 45.8293 mL/50mL
Packaging
- 50 mL in 1 BOTTLE, SPRAY (83021-400-50)
Packages (1)
Ingredients (3)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "049fe4c2-996a-198f-e063-6294a90a40b9", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "upc": ["8436019954379"], "unii": ["ZY81Z83H0X", "M629807ATL", "059QF0KO0R"], "spl_set_id": ["ebf4b3ab-34e1-185a-e053-2a95a90ace3a"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["ANUBIS COSMETICS SL"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 mL in 1 BOTTLE, SPRAY (83021-400-50)", "package_ndc": "83021-400-50", "marketing_end_date": "20270510", "marketing_start_date": "20221026"}], "brand_name": "AnubisMed", "product_id": "83021-400_049fe4c2-996a-198f-e063-6294a90a40b9", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "83021-400", "generic_name": "Sodium Bicarbonate, Aloe Barbadensis Leaf Juice, Imidazolidinyl Urea", "labeler_name": "ANUBIS COSMETICS SL", "product_type": "HUMAN OTC DRUG", "brand_name_base": "AnubisMed", "active_ingredients": [{"name": "ALOE VERA LEAF", "strength": ".15 g/50mL"}, {"name": "IMIDUREA", "strength": ".25 g/50mL"}, {"name": "WATER", "strength": "45.8293 mL/50mL"}], "application_number": "M016", "marketing_category": "OTC MONOGRAPH FINAL", "marketing_end_date": "20270510", "marketing_start_date": "20221026"}