deflame

Generic: allantoin

Labeler: noon aesthetics m.r. ltd
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name deflame
Generic Name allantoin
Labeler noon aesthetics m.r. ltd
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

allantoin 5 mg/mL

Manufacturer
Noon Aesthetics M.R. Ltd

Identifiers & Regulatory

Product NDC 78863-1270
Product ID 78863-1270_2b739f1b-7b76-4851-a368-a52fd2b7c38e
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M020
Listing Expiration 2026-12-31
Marketing Start 2023-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 788631270
Hyphenated Format 78863-1270

Supplemental Identifiers

RxCUI
241509
UNII
344S277G0Z

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 deflame (source: ndc)
Generic Name allantoin (source: ndc)
Application Number M020 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (78863-1270-1) / 50 mL in 1 TUBE
source: ndc

Packages (1)

78863-1270-1 1 TUBE in 1 CARTON (78863-1270-1) / 50 mL in 1 TUBE

Ingredients (1)

allantoin (5 mg/mL)

Linked Drug Pages (1)

DeFlame ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "2b739f1b-7b76-4851-a368-a52fd2b7c38e", "openfda": {"unii": ["344S277G0Z"], "rxcui": ["241509"], "spl_set_id": ["2628bd73-0ca9-497b-bcd9-088444cd62be"], "manufacturer_name": ["Noon Aesthetics M.R. Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (78863-1270-1)  / 50 mL in 1 TUBE", "package_ndc": "78863-1270-1", "marketing_start_date": "20231001"}], "brand_name": "DeFlame", "product_id": "78863-1270_2b739f1b-7b76-4851-a368-a52fd2b7c38e", "dosage_form": "CREAM", "product_ndc": "78863-1270", "generic_name": "ALLANTOIN", "labeler_name": "Noon Aesthetics M.R. Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "DeFlame", "active_ingredients": [{"name": "ALLANTOIN", "strength": "5 mg/mL"}], "application_number": "M020", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20231001", "listing_expiration_date": "20261231"}