FDA.reportPublic FDA data

Texture ID Anti Dandruff Peppermint Oil and Aloe

Manufacturer
RNA PHARMA, LLC
Effective date
2025-12-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:22:10

Label at a glance#

ProductTexture ID Anti Dandruff Peppermint Oil and Aloe
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTSINACTIVE INGREDIENTS

OTC - PURPOSE SECTION

PURPOSEPURPOSE

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDRENKEEP OUT OF REACH OF CHILDREN

INDICATIONS & USAGE SECTION

INDICATIONSINDICATIONS

WARNINGS SECTION

WARNINGSWARNINGS

DOSAGE & ADMINISTRATION SECTION

DOSAGESDOSAGES

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY AREAPRINCIPAL DISPLAY AREA

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
205104salicylic acid 2 % Medicated ShampooPSN1
205104salicylic acid 20 MG/ML Medicated ShampooSCD1
205104salicylic acid 2 % Medicated ConditionerSY1
205104salicylic acid 2 % Medicated ShampooSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6c13b22c-b3ba-4127-b768-0132dd5ab0d1Product name120230829
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60717-410-12Texture ID Anti Dandruff Peppermint Oil and Aloe1 g in 1 BOTTLELOTION/SHAMPOO11

Products#

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

DailyMed product names page 1 of 1 · 29 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
60717-41060717-410-12

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 28 matching rows.

Name, UNII, Kind table
NameUNIIKind
PEG-120 METHYL GLUCOSE DIOLEATEYM0K64F20VIACT
PHENOXYETHANOLHIE492ZZ3TIACT
MATRICARIA CHAMOMILLA FLOWERING TOP OILSA8AR2W4ERIACT
SODIUM CHLORIDE451W47IQ8XIACT
SODIUM BENZOATEOJ245FE5EUIACT
POLYQUATERNIUM-10 (1400 MPA.S AT 2%)W6F63XD4Z3IACT
WATER059QF0KO0RIACT
AMINOMETHYL PROPANOLLU49E6626QIACT
BENZOIC ACID8SKN0B0MIMIACT
COCO-GLUCOSIDEICS790225BIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
ISOPROPYL ALCOHOLND2M416302IACT
POTASSIUM SORBATE1VPU26JZZ4IACT
EDETATE DISODIUM7FLD91C86KIACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
BETAINE3SCV180C9WIACT
SALICYLIC ACIDO414PZ4LPZACTIB
PEPPERMINT OILAV092KU4JHIACT
GLYCERINPDC6A3C0OXIACT
SODIUM LAUROYL SARCOSINATE632GS99618IACT
CITRIC ACID2968PHW8QPIACT
GLYCERETH-2 COCOATEJWM00VS7HCIACT
HYDROXYPROPYL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDEMVW5LK6LFTIACT
POLYQUATERNIUM-70L414VCS5YIACT
ALMOND OIL66YXD4DKO9IACT
SODIUM HYDROXIDE55X04QC32IIACT
SODIUM ACETATE4550K0SC9BIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT

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
Texture ID Anti Dandruff Peppermint Oil and AloeSALICYLIC ACIDRNA PHARMA, LLC44fa5eed-93e2-cb3a-e063-6294a90a3b042025-12-02WarningsExact identifier
ndc (package): 60717-410-12
ndc (product): 60717-410
ndc11 (package): 60717041012
spl id: 44fa5eed-93e3-cb3a-e063-6294a90a3b04
spl set id: 44fa5eed-93e2-cb3a-e063-6294a90a3b04

Reported adverse events (FAERS/openFDA)#

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