triderma baby stubborn eczema itch relief

Generic: colloidal oatmeal

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

Drug Facts

Product Profile

Brand Name triderma baby stubborn eczema itch relief
Generic Name colloidal oatmeal
Labeler genuine aloe virgin corporation
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

oatmeal 1.5 g/100g

Manufacturer
Genuine Aloe Virgin Corporation

Identifiers & Regulatory

Product NDC 10738-069
Product ID 10738-069_498d0d4c-7d48-5ff0-e063-6394a90ad849
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number 505G(a)(3)
Listing Expiration 2027-12-31
Marketing Start 2019-08-30

Pharmacologic Class

Established (EPC)
non-standardized food allergenic extract [epc] non-standardized plant allergenic extract [epc]
Chemical Structure
allergens [cs] dietary proteins [cs] plant proteins [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10738069
Hyphenated Format 10738-069

Supplemental Identifiers

RxCUI
1654721
UPC
0182228000939
UNII
8PI54V663Y
NUI
N0000185371 N0000185375 N0000175629 N0000184306 M0000728 M0006342 M0016962 N0000185016

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 triderma baby stubborn eczema itch relief (source: ndc)
Generic Name colloidal oatmeal (source: ndc)
Application Number 505G(a)(3) (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.5 g/100g
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (10738-069-20) / 62 g in 1 TUBE (10738-069-25)
  • 1 TUBE in 1 CARTON (10738-069-40) / 113 g in 1 TUBE (10738-069-45)
source: ndc

Packages (2)

10738-069-20 1 TUBE in 1 CARTON (10738-069-20) / 62 g in 1 TUBE (10738-069-25) 10738-069-40 1 TUBE in 1 CARTON (10738-069-40) / 113 g in 1 TUBE (10738-069-45)

Ingredients (1)

oatmeal (1.5 g/100g)

Linked Drug Pages (1)

TRIDERMA BABY STUBBORN ECZEMA ITCH RELIEF ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "498d0d4c-7d48-5ff0-e063-6394a90ad849", "openfda": {"nui": ["N0000185371", "N0000185375", "N0000175629", "N0000184306", "M0000728", "M0006342", "M0016962", "N0000185016"], "upc": ["0182228000939"], "unii": ["8PI54V663Y"], "rxcui": ["1654721"], "spl_set_id": ["f5a83e98-da32-49ae-b81d-4279af4b154c"], "pharm_class_cs": ["Allergens [CS]", "Dietary Proteins [CS]", "Plant Proteins [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Non-Standardized Food Allergenic Extract [EPC]", "Non-Standardized Plant Allergenic Extract [EPC]"], "manufacturer_name": ["Genuine Aloe Virgin Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (10738-069-20)  / 62 g in 1 TUBE (10738-069-25)", "package_ndc": "10738-069-20", "marketing_start_date": "20190830"}, {"sample": false, "description": "1 TUBE in 1 CARTON (10738-069-40)  / 113 g in 1 TUBE (10738-069-45)", "package_ndc": "10738-069-40", "marketing_start_date": "20190830"}], "brand_name": "TRIDERMA BABY STUBBORN ECZEMA ITCH RELIEF", "product_id": "10738-069_498d0d4c-7d48-5ff0-e063-6394a90ad849", "dosage_form": "CREAM", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Dietary Proteins [CS]", "Grain Proteins [EXT]", "Increased Histamine Release [PE]", "Non-Standardized Food Allergenic Extract [EPC]", "Non-Standardized Plant Allergenic Extract [EPC]", "Plant Proteins [CS]"], "product_ndc": "10738-069", "generic_name": "Colloidal Oatmeal", "labeler_name": "Genuine Aloe Virgin Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "TRIDERMA BABY STUBBORN ECZEMA ITCH RELIEF", "active_ingredients": [{"name": "OATMEAL", "strength": "1.5 g/100g"}], "application_number": "505G(a)(3)", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20190830", "listing_expiration_date": "20271231"}