BLOOSKIM ANTI DANDRUFF- ketoconazole shampoo

BlooSkim Anti Dandruff by

Drug Labeling and Warnings

BlooSkim Anti Dandruff by is a Otc medication manufactured, distributed, or labeled by Good Manager Holdings Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ketoconazole 1%

PURPOSE

ANTI-DANDRUFF SHAMPOO

INDICATIONS & USAGE

Controls flaking, scaling, and itching caused by dandruff

WHEN USING

When using this product

Avoid contact with eyes

If contact occurs, rinse thoroughly with water.

WARNINGS

For external use only

DO NOT USE

Do not use

On scalp that is broken or inflamed

If you are allergic to ingredients in this product

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center immediately.

STOP USE

Stop use and ask a doctor if

A rash appears.

Condition worsens or does not improve within 2-4 weeks.

If pregnant or breast-feeding, consult a doctor before use.

DOSAGE & ADMINISTRATION

Directions

adults and children 12 years and over

Wet hair thoroughly.

Apply shampoo, lather generously, and rinse thoroughly.

Repeat if necessary.

Use every 3-4 days for up to 8 weeks or as directed by a doctor.

Afterward, use as needed to control dandruff.

children under 12 years

Ask a doctor

OTHER SAFETY INFORMATION

Store at 20°C to 25°C (68°F to 77°F)

INACTIVE INGREDIENT

Citric Acid, Herba Violae, Euphorbia Hirta, Murraya Paniculata , Mentha Canadensis, Sophora Flavescens, Dittany Bark, Glabrous Greenbrier Rhizome, Mosla Cavaleriei Levl, Stellera Chamaejasme, Huang Bai, Sessile Stemona Root, Gleditsia Sinensis, Common Cnidium Fruit, Fructus Kochiae, Tea Tree Oil, Water

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BLOOSKIM ANTI DANDRUFF 
ketoconazole shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82372-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
KETOCONAZOLE (UNII: R9400W927I) (KETOCONAZOLE - UNII:R9400W927I)	KETOCONAZOLE	1 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
MURRAYA PANICULATA WHOLE (UNII: Y8ZAA3Z7WU)
MENTHA CANADENSIS WHOLE (UNII: J1BO4MHT2L)
GLEDITSIA SINENSIS WHOLE (UNII: FS3UB95UTG)
WATER (UNII: 059QF0KO0R)
SMILAX GLABRA TUBER (UNII: PES3YXA3LR)
MOSLA CAVALERIEI WHOLE (UNII: 05O8B64OS2)
VIOLA PHILIPPICA WHOLE (UNII: O176VC3N54)
EUPHORBIA HIRTA (UNII: L13YF113GN)
DICTAMNUS DASYCARPUS ROOT (UNII: 6153LEN214)
TEA TREE OIL (UNII: VIF565UC2G)
STELLERA CHAMAEJASME WHOLE (UNII: 80N0P0DD9J)
SOPHORA FLAVESCENS WHOLE (UNII: X8KX602M5L)
CITRIC ACID (UNII: 2968PHW8QP)
CNIDIUM MONNIERI FRUIT (UNII: V1IA3S3CUS)
PHELLODENDRON CHINENSE WHOLE (UNII: QKA3ZK8IIE)
STEMONA SESSILIFOLIA ROOT (UNII: EKG8030U4N)
BASSIA SCOPARIA FRUIT (UNII: 04W97Z676Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82372-013-01	250 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/08/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	11/08/2024

Labeler - Good Manager Holdings Inc (118382673)