PHYTOZINE RINGWORM TREATMENT MAXIMUM STRENGTH- tolnaftate ointment 
The Sisquoc Healthcare Corporation

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Sisquoc HC (as PLD) - PHYTOZINE RINGWORM TREATMENT (71229-101)

ACTIVE INGREDIENT

TOLNAFTATE 1%

PURPOSE

ANTIFUNGAL

USES

WARNINGS

FOR EXTERNAL USE ONLY.

WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES.

STOP USE AND ASK A DOCTOR IF

DO NOT USE ON CHILDREN UNDER 2 YEARS OF AGE UNLESS DIRECTED BY A DOCTOR.

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DIRECTIONS

INACTIVE INGREDIENTS

Water, Prunus Amygdalus Dulcis (Sweet Almond) Oil, Polysorbate-20, Sodium Polyacrylate, Hydrogenated Polydecene, Trideceth-6, Glyceryl Stearate, PEG-100, Stearate, Propylene Glycol, Cetyl Alcohol, Oleth-10 Phosphate, Glycerin, Avena (Oat), Kernel Extract, Aloe Barbadensis Leaf Juice, Actrostaphylos Uva Ursi Leaf Extract, Propolis Extract, Theobroma Cacao
(Cocoa) Seed Butter, Rosa Canina Fruit Oil, Camphor, Menthol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Lavandula
Angustifolia (Lavender) Oil, Jasminum Officinale (Jasmine) Oil, Eugenia Caryophyllus (Clove) Leaf Oil, Tocopheryl
Acetate, Stearic Acid, Propylene Glycol, Butylene Glycol, Cetyl Hydroxyethylcellulose, Sodium Hydroxide, Phenoxyethanol , Ethylhexylglycerin

Store between 20°c to 25°C (68° to 77°F)

Label Phytozine Retail Proof 1-17

Insert Phytozine '17

PHYTOZINE RINGWORM TREATMENT  MAXIMUM STRENGTH
tolnaftate ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71229-101
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TOLNAFTATE (UNII: 06KB629TKV) (TOLNAFTATE - UNII:06KB629TKV) TOLNAFTATE1 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALMOND OIL (UNII: 66YXD4DKO9)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
OLETH-10 PHOSPHATE (UNII: Q95361F4VS)  
GLYCERIN (UNII: PDC6A3C0OX)  
OAT (UNII: Z6J799EAJK)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)  
PROPOLIS WAX (UNII: 6Y8XYV2NOF)  
THEOBROMA CACAO WHOLE (UNII: EB048G1S9J)  
ROSA CANINA FRUIT OIL (UNII: CR7307M3QZ)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
MENTHOL (UNII: L7T10EIP3A)  
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K)  
LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)  
JASMINUM OFFICINALE WHOLE (UNII: X3314B4SYD)  
CLOVE LEAF OIL (UNII: VCA5491KVF)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CETYL HYDROXYETHYLCELLULOSE (350000 MW) (UNII: T7SWE4S2TT)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:71229-101-1128 g in 1 TUBE; Type 0: Not a Combination Product03/25/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00503/25/2019
Labeler - The Sisquoc Healthcare Corporation (021517142)

Revised: 10/2023
Document Id: 0906e432-2f37-c2d9-e063-6394a90af9be
Set id: 5dff6ee7-f7a9-4841-8357-6b0801d253f1
Version: 4
Effective Time: 20231031
 
The Sisquoc Healthcare Corporation