DERMADIVE ULTRACARE - TETRAID- benzalkonium chloride lotion 
Releaf Technologies LLC

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RELEAF TECHNOLOGIES (as PLD) - DERMADIVE ULTRACARE - TETRAID (78663-102)

ACTIVE INGREDIENT

BENZALKONIUM CHLORIDE 0.13%

PURPOSE

ANTIMICROBIAL

USES

TO PROTECT SKIN AND SPEED HEALING OF WOUNDS AND SORES.

WARNING

FOR EXTERNAL USE ONLY.

DO NOT USE ON DEEP PUNCTURE WOUNDS OR LACERATIONS.

WHEN USING THIS PRODUCT AVOID CONTACT WITH THE EYES.

STOP USING AND ASK A DOCTOR IF

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

DIRECTIONS

APPLY AS NEEDED TO AFFECTED AREAS.

OTHER INFORMATION

PROTECT PRODUCT FROM EXCESSIVE MOISTURE - AVOID STORING IN DIRECT SUNLIGHT - STORE WITH LID TIGHTLY CLOSED.

INACTIVE INGREDIENTS

PURIFIED WATER, GLYCERYL STEARATE, EMULSIFYING WAX, STEARYL ALCOHOL, CETYL ALCOHOL, CYCLOTETRASILOXANE (AND) CYCLOPENTASILOXANE, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, ETHOXYDIGLYCOL, PROPYLENE GLYCOL, WATER, LECITHIN, ALCOHOL, GLYCERIN, TEA TREE OIL, TRIETHANOLAMINE

01b LBL_Tetraid_100mL

DERMADIVE ULTRACARE - TETRAID 
benzalkonium chloride lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78663-102
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE0.13 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
WATER (UNII: 059QF0KO0R)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
TROLAMINE (UNII: 9O3K93S3TK)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
CYCLOMETHICONE 4 (UNII: CZ227117JE)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
TEA TREE OIL (UNII: VIF565UC2G)  
ALCOHOL (UNII: 3K9958V90M)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:78663-102-34100 mL in 1 TUBE; Type 0: Not a Combination Product08/07/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM00308/07/2023
Labeler - Releaf Technologies LLC (117532647)

Revised: 11/2023
Document Id: 0942d1fe-062f-62fd-e063-6394a90a871e
Set id: 025c0b33-73ca-334b-e063-6394a90ad668
Version: 2
Effective Time: 20231103
 
Releaf Technologies LLC