Package 49967-895-02

Brand: kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment

Generic: sulfur
NDC Package

Package Facts

Identity

Package NDC 49967-895-02
Digits Only 4996789502
Product NDC 49967-895
Product ID 49967-895_1cb9aca2-b493-4ee2-85c9-0001329654fc
Description

3 mL in 1 PACKET (49967-895-02)

Marketing

Marketing Status
Marketed Since 2016-11-01
Brand kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment
Generic sulfur
Sample Package No

Linked Drug Pages (1)

Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "1cb9aca2-b493-4ee2-85c9-0001329654fc", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["240725"], "spl_set_id": ["217c697e-0260-46d5-a202-ce7345eadd94"], "manufacturer_name": ["L'Oreal USA Products Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (49967-895-01)  / 20 mL in 1 TUBE", "package_ndc": "49967-895-01", "marketing_start_date": "20161101"}, {"sample": false, "description": "3 mL in 1 PACKET (49967-895-02)", "package_ndc": "49967-895-02", "marketing_start_date": "20161101"}, {"sample": false, "description": "1.5 mL in 1 PACKET (49967-895-03)", "package_ndc": "49967-895-03", "marketing_start_date": "20161101"}, {"sample": false, "description": "3 mL in 1 TUBE (49967-895-04)", "package_ndc": "49967-895-04", "marketing_start_date": "20161101"}], "brand_name": "Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment", "product_id": "49967-895_1cb9aca2-b493-4ee2-85c9-0001329654fc", "dosage_form": "LOTION", "product_ndc": "49967-895", "generic_name": "Sulfur", "labeler_name": "L'Oreal USA Products Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment", "active_ingredients": [{"name": "SULFUR", "strength": "100 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20161101", "listing_expiration_date": "20261231"}