glovers dandruff control medicine, regular
Generic: sulfur
Labeler: j. strickland & co.Drug Facts
Product Profile
Brand Name
glovers dandruff control medicine, regular
Generic Name
sulfur
Labeler
j. strickland & co.
Dosage Form
SUSPENSION
Routes
Active Ingredients
sulfur 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
12022-007
Product ID
12022-007_08340897-23b3-f23b-e063-6294a90a4eb9
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M032
Listing Expiration
2026-12-31
Marketing Start
2001-09-24
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
12022007
Hyphenated Format
12022-007
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
glovers dandruff control medicine, regular (source: ndc)
Generic Name
sulfur (source: ndc)
Application Number
M032 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 BOTTLE in 1 CARTON (12022-007-00) / 81 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "08340897-23b3-f23b-e063-6294a90a4eb9", "openfda": {"upc": ["0310471011437"], "unii": ["70FD1KFU70"], "rxcui": ["247683"], "spl_set_id": ["18700036-11ec-4370-bcc6-b9e2c732e7d9"], "manufacturer_name": ["J. Strickland & Co."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (12022-007-00) / 81 mL in 1 BOTTLE", "package_ndc": "12022-007-00", "marketing_start_date": "20010924"}], "brand_name": "Glovers Dandruff Control Medicine, Regular", "product_id": "12022-007_08340897-23b3-f23b-e063-6294a90a4eb9", "dosage_form": "SUSPENSION", "product_ndc": "12022-007", "generic_name": "Sulfur", "labeler_name": "J. Strickland & Co.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Glovers Dandruff Control Medicine, Regular", "active_ingredients": [{"name": "SULFUR", "strength": "25 mg/mL"}], "application_number": "M032", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20010924", "listing_expiration_date": "20261231"}