FDA.reportPublic FDA data

Doo Gro Braids Twists Locs Dandruff Control Moisturizing Spray

Manufacturer
J. Strickland and Co.
Effective date
2024-02-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:13:09

Label at a glance#

ProductDoo Gro Braids Twists Locs Dandruff Control Moisturizing
Active ingredientSALICYLIC ACID
Label structure6 sections

Dosage and administration

Spray to apply to the affected areas 1-4 times daily, or as directed by a doctor.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid, 2%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use:

INDICATIONS & USAGE SECTION

Controls scalp itching and flaking due to dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and consult a doctor

OTC - STOP USE SECTION

  • if condition worsens or does not improve after regular use of this product as directed.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or call a poison control center at once.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Spray to apply to the affected areas 1-4 times daily, or as directed by a doctor.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, Glycerin, PEG-12 Dimethicone, Propylene Glycol, Sodium Hydroxide, Hydrolyzed Collagen, Disodium EDTA, Diazolidinyl Urea, Methylparaben, Propylparaben, Benzyl Alcohol, Benzyl Benzoate, Eugenol, Hydroxycitronellal, Linalool, Fragrance.

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1048903salicylic acid 2 % Topical SprayPSN1
1048903salicylic acid 20 MG/ML Topical SpraySCD1
1048903salicylic acid 2 % Topical SpraySY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
12022-041-00Doo Gro Braids Twists Locs Dandruff Control Moisturizing335 mL in 1 BOTTLELIQUID3351

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12022-041DOO GRO BRAIDS TWISTS LOCS DANDRUFF CONTROL MOISTURIZING (SALICYLIC ACID) LIQUID [J. STRICKLAND AND CO.]1Current NDC, 1 package rows20240601_116f4f0d-66c7-49dd-e063-6394a90ab2b5.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
12022-04112022-041-00

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
GLYCERINPDC6A3C0OXIACT
PEG-12 DIMETHICONEZEL54N6W95IACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SODIUM HYDROXIDE55X04QC32IIACT
EDETATE DISODIUM7FLD91C86KIACT
DIAZOLIDINYL UREAH5RIZ3MPW4IACT
METHYLPARABENA2I8C7HI9TIACT
PROPYLPARABENZ8IX2SC1OHIACT
BENZYL ALCOHOLLKG8494WBHIACT
BENZYL BENZOATEN863NB338GIACT
EUGENOL3T8H1794QWIACT
HYDROXYCITRONELLAL8SQ0VA4YURIACT
LINALOOL, (+/-)-D81QY6I88EIACT
SALICYLIC ACIDO414PZ4LPZACTIB

Source Document#

Source XML

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Doo Gro Braids Twists Locs Dandruff Control MoisturizingSALICYLIC ACIDJ. Strickland and Co.116f4f0d-66c7-49dd-e063-6394a90ab2b52024-02-15WarningsExact identifier
ndc (package): 12022-041-00
ndc (product): 12022-041
ndc11 (package): 12022004100
spl id: 116f484f-866f-4840-e063-6394a90a11e9
spl set id: 116f4f0d-66c7-49dd-e063-6394a90ab2b5

Reported adverse events (FAERS/openFDA)#

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