spot correction

Generic: sulfur

Labeler: hydropeptide llc
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name spot correction
Generic Name sulfur
Labeler hydropeptide llc
Dosage Form CREAM
Routes
TOPICAL
Active Ingredients

sulfur 30 mg/mL

Manufacturer
HydroPeptide LLC

Identifiers & Regulatory

Product NDC 60934-002
Product ID 60934-002_0c0ec51d-1cf2-a16d-e063-6294a90afd94
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M006
Listing Expiration 2026-12-31
Marketing Start 2017-01-11

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 60934002
Hyphenated Format 60934-002

Supplemental Identifiers

RxCUI
199632
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 spot correction (source: ndc)
Generic Name sulfur (source: ndc)
Application Number M006 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 30 mg/mL
source: ndc
Packaging
  • 1 TUBE in 1 BOX (60934-002-01) / 15 mL in 1 TUBE
source: ndc

Packages (1)

60934-002-01 1 TUBE in 1 BOX (60934-002-01) / 15 mL in 1 TUBE

Ingredients (1)

sulfur (30 mg/mL)

Linked Drug Pages (1)

Spot Correction ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "0c0ec51d-1cf2-a16d-e063-6294a90afd94", "openfda": {"unii": ["70FD1KFU70"], "rxcui": ["199632"], "spl_set_id": ["45ec40ff-7134-085b-e054-00144ff8d46c"], "manufacturer_name": ["HydroPeptide LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 BOX (60934-002-01)  / 15 mL in 1 TUBE", "package_ndc": "60934-002-01", "marketing_start_date": "20170111"}], "brand_name": "Spot Correction", "product_id": "60934-002_0c0ec51d-1cf2-a16d-e063-6294a90afd94", "dosage_form": "CREAM", "product_ndc": "60934-002", "generic_name": "SULFUR", "labeler_name": "HydroPeptide LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Spot Correction", "active_ingredients": [{"name": "SULFUR", "strength": "30 mg/mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170111", "listing_expiration_date": "20261231"}