nasal dryness relief gel

Generic: allantoin

Labeler: genuine virgin aloe corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name nasal dryness relief gel
Generic Name allantoin
Labeler genuine virgin aloe corporation
Dosage Form GEL
Routes
TOPICAL
Active Ingredients

allantoin .5 g/100g

Manufacturer
Genuine Virgin Aloe Corporation

Identifiers & Regulatory

Product NDC 10738-051
Product ID 10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2022-05-20

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10738051
Hyphenated Format 10738-051

Supplemental Identifiers

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 nasal dryness relief gel (source: ndc)
Generic Name allantoin (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • .5 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15)
source: ndc

Packages (1)

10738-051-10 1 TUBE in 1 CARTON (10738-051-10) / 28 g in 1 TUBE (10738-051-15)

Ingredients (1)

allantoin (.5 g/100g)

Linked Drug Pages (1)

Nasal Dryness Relief Gel ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "49655e27-0a67-4fca-e063-6294a90a5cfa", "openfda": {"unii": ["344S277G0Z"], "spl_set_id": ["dfece059-57bd-8eee-e053-2a95a90a980e"], "manufacturer_name": ["Genuine Virgin Aloe Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10738-051-10)  / 28 g in 1 TUBE (10738-051-15)", "package_ndc": "10738-051-10", "marketing_start_date": "20220520"}], "brand_name": "Nasal Dryness Relief Gel", "product_id": "10738-051_49655e27-0a67-4fca-e063-6294a90a5cfa", "dosage_form": "GEL", "product_ndc": "10738-051", "generic_name": "Allantoin", "labeler_name": "Genuine Virgin Aloe Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Nasal Dryness Relief Gel", "active_ingredients": [{"name": "ALLANTOIN", "strength": ".5 g/100g"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220520", "listing_expiration_date": "20271231"}