Version X Scalp Tonic

Manufacturer
CHRISTLTD
Effective date
2013-05-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 22:35:28

Label at a glance#

ProductVersion X Scalp Tonic
Active ingredientAllantoin
Label structure8 sections

Indications and uses

DIRECTIONS Apply directly to clean, towel-dried scalp. Spray the stimulant to the affected and surrounding areas of the scalp once daily. Gently massage the stimulant into the scalp for 10-20 seconds. Do not wash or rinse hair for at least three hours. For best results continue use on a daily basis.

Dosage and administration

DIRECTIONS Apply directly to clean, towel-dried scalp. Spray the stimulant to the affected and surrounding areas of the scalp once daily. Gently massage the stimulant into the scalp for 10-20 seconds. Do not wash or rinse hair for at least three hours. For best results continue use on a daily basis.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredient: Allantoin 0.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:
Water,SD Alcohol 40-B,Butylene Glycol,Nonoxynol-12,Propylene Glycol,Panthenol,Fragrance,0.3H0.1ydrolyzed Soy Protein,DMDM Hydantoin,Menthol,Peg-60 Almond Glycerides,Hair Keratin, Amino Acids,Sodium Chondroitin Sulfate,3-Aminopropane Sulfonic Acid,Chlorphenesin, Xantham Gum,PG-Propyl Silanetriol,Hydrolyzed Wheat Protein,Ethyl Nicotinate,Benzophenone-4, Sodium PCA,Yellow 6 (CI 15985),Red 40 (CI 16035),Blue 1 (CI 42090),Sodium Chloride,Disodium EDTA,Alcohol,Cetyl Triethylmonium Dimethicone PEG-8phthalate,Ginkgo Biloba Leaf Extract,Swertia Japonica Extract,Laminaria Digitata Extract,Pelvetia Canaliculata Extract,Anacyclus Pyrethrum, Root Extract,Beta Vulgaris (Beet) Root Extract,Adiantum Pedatum Extract,Flower Extract, Eugenia Caryophyllus (Clove),Hedychium CoronariumRoot Extract,Arnica Montana Flower Extract, Urtica Dioica (Nettle) Extract,Rosmarinus Officinalis(Rosemary) Leaf Extract,Shell Extract,Juglans Nigra(Black Walnut),Salvia Officinalis (Sage) Leaf Extract, Hamamelis Virginiana,Quillaja Saponaria Bark Extract,Algae Extract,Phytantriol,Biotin,Niacin,Retinyl Palmitate, Tocopheryl Nicotinate

PURPOSE

OTC - PURPOSE SECTION

Purpose: Skin Protectant

WARNINGS

WARNINGS SECTION

CAUTION:
For external use only.
Avoid eye contact.
Keep out of reach children.
In case of accidental ingestion, seek professional attention immediately.
Some redness and iffitation of the scalp is nomal

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN

INDICATIONS AND USAGE

INDICATIONS & USAGE SECTION

DIRECTIONS
Apply directly to clean, towel-dried scalp.
Spray the stimulant to the affected and surrounding areas of the scalp once daily.
Gently massage the stimulant into the scalp for 10-20 seconds.
Do not wash or rinse hair for at least three hours. For best results continue use on a daily basis.

DOSAGE AND ADMINISTRATION

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS
Apply directly to clean, towel-dried scalp.
Spray the stimulant to the affected and surrounding areas of the scalp once daily.
Gently massage the stimulant into the scalp for 10-20 seconds.
Do not wash or rinse hair for at least three hours. For best results continue use on a daily basis.

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
58069-010-012019-11-27C16284748780-19855d018-dfdf-cd31-e053-dbdaa90ab51a3ff15154-bdb0-4082-aaf8-79c2564eca63

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58069-010-01Version X Scalp Tonic125 mL in 1 CARTONLIQUID1252

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58069-010VERSION X SCALP TONIC (ALLANTOIN) LIQUID [CHRISTLTD]2Legacy NDC, 1 package rows20130521_3ff15154-bdb0-4082-aaf8-79c2564eca63.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
AllantoinACTIVE INGREDIENT344S277G0Z2
ALLANTOINACTIVE MOIETY344S277G0Z2
Butylene GlycolINACTIVE INGREDIENT3XUS85K0RA2
PanthenolINACTIVE INGREDIENTWV9CM0O67Z2
WaterINACTIVE INGREDIENT059QF0KO0R2

Products#

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

DailyMed product names page 1 of 1 · 5 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58069-01058069-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 2 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TOPICAL1400 mgExact identifier — unii candidate
2 equally ranked IID candidates
Butylene GlycolBUTYLENE GLYCOL3XUS85K0RASYSTEM / TRANSDERMAL8.12 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
7b51f02c-9e36-4469-97ac-c6baec73b6fe3ff15154-bdb0-4082-aaf8-79c2564eca632013-05-21WarningsExact identifier
spl id: 7b51f02c-9e36-4469-97ac-c6baec73b6fe
spl set id: 3ff15154-bdb0-4082-aaf8-79c2564eca63

Reported adverse events (FAERS/openFDA)#

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