FDA.reportPublic FDA data

Avalon Organics Antidandruff

Manufacturer
The Hain Celestial Group, Inc.
Effective date
2025-07-11
Label type
HUMAN OTC DRUG LABEL
Version
11
Source
full-release
Hydrated at
2026-06-01 01:07:08

Label at a glance#

ProductAvalon Organics Antidandruff
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION



For external use only. Avoid contact with eyes. Rinse eyes throughly with water in case contact ossurs. Discontinue to use and contact your physician if irritation develops.

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 2.0%

OTC - PURPOSE SECTION

Controls symptoms of dandruff, seboric dermatitis and psoriasis

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

INDICATIONS & USAGE SECTION

For relief of flaking, scaling and itching associated with dandruff. Helps prevent seborrheic dermatitis

DOSAGE & ADMINISTRATION SECTION

For the best results use at least three times each week. Wet hair, lather, massage onto scalp. Rinse and repeat if desired.

INACTIVE INGREDIENT SECTION

Aloe Barbadensis Leaf Juice (1), Sodium Coco-Sulfate, Coco-Glucoside, Sodium Laurylglucosides Hydroxypropylsulfonate, Glyceryl Oleate, Cedrus Atlantica Bark Oil, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Copaifera Officinalis (Balsam Copaiba) Resin, Coriandrum Sativum (Coriander) Fruit Oil, Geranium Maculatum Oil, Lavandula Angustifolia (Lavender) Oil, Melaleuca Alternifolia (Tea Tree) Leaf Oil (1), Mentha Arvensis Leaf Oil, Mentha Piperita (Peppermint) Oil, Pogostemon Cablin Oil, Rosmarinus Officinalis (Rosemary) Leaf Oil, Chamomilla Recutita (Matricaria) Flower Extract (1), Chenopodium Quinoa Seed (1), Rosmarinus Officinalis (Rosemary) Leaf Extract (1), Styrax Benzoin Resin Extract, Tocopheryl Acetate, Bisabolol, Citric Acid, Disodium Cocoyl Glutamate, Inulin (1), Menthol, Potassium Hydroxide, Sodium Chloride, Sodium Phytate, Sodium Sulfate, Water (Aqua), Alcohol, Benzyl Alcohol, Potassium Sorbate, Sodium Benzoate, Limonene, Linalool.

(1) Certified Organic Ingredient

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

AV36106 LabelAV36106 Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
362d7abb-94e6-4c60-9a58-266894157713Product name120231023

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
61995-1606-82024-07-31C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml
61995-1606-82024-07-30C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml
61995-1606-82023-12-06C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml
61995-1606-82023-01-30C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml
61995-1606-82021-02-28C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml
61995-1606-82021-01-29C16284748780-1ba0f9c33-470d-a910-e053-dadaa90a0b85Avalon Organic Anti-dandruff Shampoo 153-067C, F01866 Items: AV36106 414g, AV35009 325ml

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
61995-1606-8Avalon Organics Antidandruff414 g in 1 BOTTLESHAMPOO41411
61995-1606-9Avalon Organics Antidandruff325 g in 1 BOTTLESHAMPOO32511

Products#

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

DailyMed product names page 1 of 1 · 40 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
61995-160661995-1606-8, 61995-1606-9

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 39 matching rows.

Name, UNII, Kind table
NameUNIIKind
GERANIUM MACULATUM ROOT OILH2E371EDYXIACT
GLYCERYL OLEATE4PC054V79PIACT
LIMONENE, (+/-)-9MC3I34447IACT
SODIUM COCO-SULFATE3599J29ANHIACT
DISODIUM COCOYL GLUTAMATEMBK0CP8F5AIACT
LINALOOL, (+/-)-D81QY6I88EIACT
COCO GLUCOSIDEICS790225BIACT
SODIUM SULFATE0YPR65R21JIACT
ALOE VERA LEAFZY81Z83H0XIACT
WATER059QF0KO0RIACT
CHAMOMILEFGL3685T2XIACT
MELALEUCA ALTERNIFOLIA LEAFG43C57162KIACT
ROSMARINUS OFFICINALIS FLOWERNR1A27F29OIACT
STYRAX BENZOIN RESINFE663Z8IROIACT
CEDRUS ATLANTICA BARK OILZX5QRE4U60IACT
ORANGE OILAKN3KSD11BIACT
LEMON OILI9GRO824LLIACT
COPAIFERA OFFICINALIS RESIN1VH544O5ATIACT
CORIANDER OIL7626GC95E5IACT
LAVENDER OILZBP1YXW0H8IACT
MENTHA ARVENSIS LEAF OIL1AEY1M553NIACT
MENTHA PIPERITA79M2M2UDA9IACT
POGOSTEMON CABLIN WHOLEH6UKY25H2PIACT
ROSEMARY OIL8LGU7VM393IACT
.ALPHA.-BISABOLOL, (+)-105S6I733ZIACT
INULINJOS53KRJ01IACT
MENTHOLL7T10EIP3AIACT
POTASSIUM HYDROXIDEWZH3C48M4TIACT
.ALPHA.-TOCOPHEROL ACETATE9E8X80D2L0IACT
ALCOHOL3K9958V90MIACT
BENZYL ALCOHOLLKG8494WBHIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
SODIUM BENZOATEOJ245FE5EUIACT
SALICYLIC ACIDO414PZ4LPZACTIB
CHENOPODIUM QUINOA SEEDOO4K72NZ2XIACT
SODIUM CHLORIDE451W47IQ8XIACT
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
HEXASODIUM PHYTATEZBX50UG81VIACT

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
Avalon Organics AntidandruffSALICYLIC ACIDThe Hain Celestial Group, Inc.66c7f730-64f3-4eef-e053-2a91aa0a42252025-07-11WarningsExact identifier
ndc (package): 61995-1606-8
ndc (package): 61995-1606-9
ndc (product): 61995-1606
ndc11 (package): 61995160608
ndc11 (package): 61995160609
spl id: 39ae13bf-c20b-a955-e063-6294a90a7302
spl set id: 66c7f730-64f3-4eef-e053-2a91aa0a4225

Reported adverse events (FAERS/openFDA)#

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