Package 59088-326-07

Brand: Scartrate Cream

Generic: Dimethicone, Allantoin
NDC Package

Package Facts

Identity

Package NDC 59088-326-07
Digits Only 5908832607
Product NDC 59088-326
Description

85 g in 1 TUBE (59088-326-07)

Marketing

Marketing Status
Discontinued 2026-02-28
Brand Scartrate Cream
Generic Dimethicone, Allantoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "34956207-efbf-efdb-e063-6394a90a3b91", "openfda": {"nui": ["N0000010282"], "unii": ["344S277G0Z", "92RU3N3Y1O"], "spl_set_id": ["1d666463-8294-5f78-e063-6294a90a91a7"], "pharm_class_pe": ["Skin Barrier Activity [PE]"], "manufacturer_name": ["Puretek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "85 g in 1 TUBE (59088-326-07)", "package_ndc": "59088-326-07", "marketing_end_date": "20260228", "marketing_start_date": "20240718"}], "brand_name": "Scartrate Cream", "product_id": "59088-326_34956207-efbf-efdb-e063-6394a90a3b91", "dosage_form": "CREAM", "pharm_class": ["Skin Barrier Activity [PE]"], "product_ndc": "59088-326", "generic_name": "Dimethicone, Allantoin", "labeler_name": "Puretek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Scartrate Cream", "active_ingredients": [{"name": "ALLANTOIN", "strength": "22.5 mg/g"}, {"name": "DIMETHICONE", "strength": "50 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_end_date": "20260228", "marketing_start_date": "20240718"}