GM COLLIN SPF 25 UVA - UVB URBAN PROTECTION VEIL SUNSCREEN- zinc oxide and titanium dioxide cream 
Laboratoires Dermo-Cosmetik Inc.

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GM Collin ®
SPF 25 UVA - UVB Urban Protection Veil

Product Facts / Drug Facts

Active ingredients:Purpose
Zinc Oxide 13.3%Sunscreen
Titanium Dioxide 3.8%Sunscreen

Uses

Warnings

For external use only. Shake well before each use.

Do not useon damaged or broken skin.

When using this productkeep out of eyes. Rinse with water to remove.

Stop use and ask a doctorif rash occurs.

Keep out of reach of children.

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

Directions

Adults over 18 years old:

Other information

Inactive ingredients

1,2-HEXANEDIOL, ALUMINA, AQUA/WATER/EAU, ARGANIA SPINOSA KERNEL OIL, ASCORBYL PALMITATE, BISABOLOL, C12-15 ALKYL BENZOATE, FARNESOL, FRAGRANCE/PARFUM, HYDROGEN DIMETHICONE, ISODECYL LAURATE, MAGNESIUM SULFATE, NEOPENTYL GLYCOL DIETHYLHEXANOATE, PHENOXYETHANOL, POLYGLYCERYL-6 POLYHYDROXYSTEARATE, POLYGLYCERYL-6 POLYRICINOLEATE, POLYHYDROXYSTEARIC ACID, POTASSIUM SORBATE, PROPANEDIOL DICAPRYLATE, TOCOPHEROL, TOCOPHERYL ACETATE, TRIETHOXYCAPRYLYLSILANE.

Questions?

USA: 1 (800) 341-1531 / CANADA: 1 (800) 361-1263

DISTRIBUTED BY:
® LABORATOIRES DERMO-COSMETIK INC.
68 STINSON, MONTREAL, QUEBEC, CANADA H4N 2E7

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box

G.M. COLLIN ®

C

SPF
25
UVA∙UVB

URBAN PROTECTION VEIL

Broad Spectrum
Mineral Sunscreen

NDC 64127-234-01
NPN 801xxxxx
06886

100 ml - 3.4 fl. oz.

PRINCIPAL DISPLAY PANEL - 100 ml Bottle Box
GM COLLIN  SPF 25 UVA - UVB URBAN PROTECTION VEIL SUNSCREEN
zinc oxide and titanium dioxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:64127-234
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE14.6 mg  in 100 mL
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE4.2 mg  in 100 mL
Inactive Ingredients
Ingredient NameStrength
1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
WATER (UNII: 059QF0KO0R)  
ARGAN OIL (UNII: 4V59G5UW9X)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
LEVOMENOL (UNII: 24WE03BX2T)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
FARNESOL (UNII: EB41QIU6JL)  
ISODECYL LAURATE (UNII: 254BX4O0JU)  
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
PROPANEDIOL DICAPRYLATE (UNII: C577OMC6UH)  
TOCOPHEROL (UNII: R0ZB2556P8)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:64127-234-011 in 1 BOX01/15/2021
1100 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02001/15/2021
Labeler - Laboratoires Dermo-Cosmetik Inc. (249335480)
Establishment
NameAddressID/FEIBusiness Operations
Dermolab Pharma Ltd245414743manufacture(64127-234)

Revised: 10/2023
Document Id: 07d92a69-05da-5394-e063-6294a90a4229
Set id: 4f0d44ca-09f0-4feb-b78c-77d83e75d4e2
Version: 3
Effective Time: 20231027
 
Laboratoires Dermo-Cosmetik Inc.