kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment

Generic: sulfur

Labeler: l'oreal usa products inc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment
Generic Name sulfur
Labeler l'oreal usa products inc
Dosage Form LOTION
Routes
TOPICAL
Active Ingredients

sulfur 100 mg/mL

Manufacturer
L'Oreal USA Products Inc

Identifiers & Regulatory

Product NDC 49967-895
Product ID 49967-895_1cb9aca2-b493-4ee2-85c9-0001329654fc
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M006
Listing Expiration 2026-12-31
Marketing Start 2016-11-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49967895
Hyphenated Format 49967-895

Supplemental Identifiers

RxCUI
240725
UNII
70FD1KFU70

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 kiehls since 1851 dermatologist solutions breakout control targeted acne spot treatment (source: ndc)
Generic Name sulfur (source: ndc)
Application Number M006 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 CARTON (49967-895-01) / 20 mL in 1 TUBE
  • 3 mL in 1 PACKET (49967-895-02)
  • 1.5 mL in 1 PACKET (49967-895-03)
  • 3 mL in 1 TUBE (49967-895-04)
source: ndc

Packages (4)

49967-895-01 1 TUBE in 1 CARTON (49967-895-01) / 20 mL in 1 TUBE 49967-895-02 3 mL in 1 PACKET (49967-895-02) 49967-895-03 1.5 mL in 1 PACKET (49967-895-03) 49967-895-04 3 mL in 1 TUBE (49967-895-04)

Ingredients (1)

sulfur (100 mg/mL)

Linked Drug Pages (1)

Kiehls Since 1851 Dermatologist Solutions Breakout Control Targeted Acne Spot Treatment ndc-match (0.9)

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"}