acnecare dermacontrol cream
Generic: salicylic acid
Labeler: spa de soleilDrug Facts
Product Profile
Brand Name
acnecare dermacontrol cream
Generic Name
salicylic acid
Labeler
spa de soleil
Dosage Form
LIQUID
Routes
Active Ingredients
benzoyl peroxide 3 mg/60mL
Manufacturer
Identifiers & Regulatory
Product NDC
68062-8090
Product ID
68062-8090_48e03804-adc2-54dc-e063-6294a90a94f5
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M006
Listing Expiration
2027-12-31
Marketing Start
2022-12-23
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680628090
Hyphenated Format
68062-8090
Supplemental Identifiers
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
acnecare dermacontrol cream (source: ndc)
Generic Name
salicylic acid (source: ndc)
Application Number
M006 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3 mg/60mL
Packaging
- 60 mL in 1 TUBE (68062-8090-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "48e03804-adc2-54dc-e063-6294a90a94f5", "openfda": {"unii": ["W9WZN9A0GM"], "spl_set_id": ["f08401ce-bb52-3e6b-e053-2995a90ad595"], "manufacturer_name": ["Spa de Soleil"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 TUBE (68062-8090-1)", "package_ndc": "68062-8090-1", "marketing_start_date": "20221223"}], "brand_name": "Acnecare Dermacontrol Cream", "product_id": "68062-8090_48e03804-adc2-54dc-e063-6294a90a94f5", "dosage_form": "LIQUID", "product_ndc": "68062-8090", "generic_name": "salicylic acid", "labeler_name": "Spa de Soleil", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acnecare Dermacontrol Cream", "active_ingredients": [{"name": "BENZOYL PEROXIDE", "strength": "3 mg/60mL"}], "application_number": "M006", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20221223", "listing_expiration_date": "20271231"}