FDA.reportPublic FDA data

RestoraScalp Anti Dandruff Dry Light Roots

Product NDC
84042-101
11-digit product format
840420101
Labeler code
84042
Product ID
84042-101_5bdc88e2-b0c1-bf88-e063-6394a90af626
Type
HUMAN OTC DRUG
Nonproprietary name
Anti Dandruff Dry Shampoo
Dosage form
POWDER
Route
TOPICAL
Labeler
Raven Innovations LLC
Application
M032
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2024-09-16
Substance
SALICYLIC ACID
Active strength
2 g/100g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage84042-10184042-101-01DDiscontinued by firm2026-10-15

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
RestoraScalp Anti Dandruff Dry Light Roots
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SALICYLIC ACID2 g/100g

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84042-101-01RestoraScalp Anti Dandruff Dry Light Roots35 g in 1 BOTTLEPOWDER351

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84042-101RESTORASCALP ANTI DANDRUFF DRY LIGHT ROOTS (ANTI DANDRUFF DRY SHAMPOO) POWDER [RAVEN INNOVATIONS LLC]1Current NDC, 1 package rows20240917_1ce9f1e1-4119-1f32-e063-6294a90a9fe0.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 31 of 31 · 615 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Sulfur 8 Light Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.d8f9afe8-bc44-41be-806b-b77d2def0fb02023-10-21WarningsExact identifier
application number: M032
Glovers Dandruff Control Medicine, RegularSULFURJ. Strickland & Co.18700036-11ec-4370-bcc6-b9e2c732e7d92023-10-21WarningsExact identifier
application number: M032
Glovers Medicated Anti-Dandruff ScalpSALICYLIC ACIDJ. Strickland & Co.bdf40a16-7b40-497e-939d-366cbe62b5552023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Original Anti-Dandruff Hair and Scalp ConditionerSULFURJ. Strickland & Co.eb1d6e9e-e7fd-478e-80c0-3a3f529682d72023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Loc Twist and Braid ScalpSALICYLIC ACIDJ. Strickland & Co.1aee59aa-ed8e-4f95-be99-63ce0814c03c2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Fresh Anti-Dandruff Hair and Scalp ConditionerSALICYLIC ACIDJ. Strickland & Co.27b6276a-eaa0-4fb7-996c-53e8c28680912023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff ControlSALICYLIC ACIDJ. Strickland and Co.961ffab9-4e1b-83f3-e053-2a95a90af5fe2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing TreatmentSALICYLIC ACIDJ. Strickland and Co.96b24a6f-3d6e-6d60-e053-2a95a90a83302023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil SerumSULFURJ. Strickland and Co.96b249a2-3f50-1ab8-e053-2995a90a56ed2023-10-21WarningsExact identifier
application number: M032
Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Butter CreamSULFUR, SALICYLIC ACIDJ. Strickland and Co.96b26d20-d4d8-1bc3-e053-2995a90afec02023-10-21WarningsExact identifier
application number: M032
Glovers Clinical Care Seborrheic Dermatitis AntidandruffPYRITHIONE ZINCJ. Strickland and Co.fef5701f-c5c7-4932-9a1c-42532e3910a52023-10-21WarningsExact identifier
application number: M032
Topco AssociatesSELENIUM SULFIDETopco Associatesecf87660-f552-1f6b-e053-2a95a90a24862023-05-04WarningsExact identifier
application number: M032
Careone Medicated DandruffSELENIUM SULFIDERetail Business Services, LLCcb05b9c6-c1bb-b210-e053-2a95a90afaea2021-08-26WarningsExact identifier
application number: M032
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-DandruffSELENIUM SULFIDEGOODSENSE21291e29-57ab-4761-8e8c-eef43ca65b242020-06-30WarningsExact identifier
application number: M032
ZolidynePYRITHIONE ZINCTopiderm, Inc.6d5eaecc-a3a1-4739-ae5b-66df4a15cd212019-11-20WarningsExact identifier
application number: M032

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
84042-101-018404201010135 g in 1 BOTTLE35 gHistorical
84042-101-028404201010217.5 g in 1 BOTTLE (84042-101-02) 17.5 g2026-09-19NoNoCurrent