anubismed

Generic: sodium bicarbonate, aloe barbadensis leaf juice, imidazolidinyl urea

Labeler: anubis cosmetics sl
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH FINAL Inactive Finished

Drug Facts

Product Profile

Brand Name anubismed
Generic Name sodium bicarbonate, aloe barbadensis leaf juice, imidazolidinyl urea
Labeler anubis cosmetics sl
Dosage Form LIQUID
Routes
TOPICAL
Active Ingredients

aloe vera leaf .15 g/50mL, imidurea .25 g/50mL, water 45.8293 mL/50mL

Manufacturer
ANUBIS COSMETICS SL

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)
standardized chemical allergen [epc]
Chemical Structure
allergens [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 83021400
Hyphenated Format 83021-400

Supplemental Identifiers

UPC
8436019954379
UNII
ZY81Z83H0X M629807ATL 059QF0KO0R
NUI
N0000185508 N0000175629 N0000184306 M0000728

Packaging Origin

Original Packager
true

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
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .15 g/50mL
  • .25 g/50mL
  • 45.8293 mL/50mL
source: ndc
Packaging
  • 50 mL in 1 BOTTLE, SPRAY (83021-400-50)
source: ndc

Packages (1)

Ingredients (3)

aloe vera leaf (.15 g/50mL) imidurea (.25 g/50mL) water (45.8293 mL/50mL)

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"}