CITY SUNSCREEN SERUM SPF 30 DOCTOR TS SUPER GOOP- homosalate, octisalate, avobenzene, octocrylene cream
Taylor James LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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City Sunscreen Serum

Active ingredients: Homosalate 8%, Octisalate 4%, Avobenzene 3%, Octocrylene 2%

Uses A light face and neck serum with three fold functions to protect skin from UVA and UVB sun exposure, stimulate repair mechanisms, and provide 24 hour moisture simultaneously. Clinical Tests with uniprotect PT-3 show significantly sings of aging including wrinkles and age spot formations.

Keep out of reach of children

Stop use and consult a physician if rash or irritation develops.

For external use only. Keep out of of eyes. Rinse with water to remove. Overexposure to the sun is a serious health threat.

Directions Apply 1-2 pumps to face and neck each morning each morning. Massage into skin and reapply after swimming or water exposure. Can be used alone or under makeup as a primer.

Inactive Ingredients Purified water (Aqua), Cyclometicone, Isostearyl Neopentanoate, Glycerin, Ceteareth-20, Polypropylene, Cetearyl Alcohol, Xanthan Gum, d-Panthenol, Octanohydroxamic acid, Caprylyl Glycol, Silica, Triacontanyl PVP, Cetyl Dimethicone, Ammonium Acryloyldimethyltaurate/VP Copolymer, PEG-40 Stearate, Tocopheryl, Disodium EDTA, Pentylene Glycol, Pantheyl Triacetate, Sodium Lactate, Lactic Acid, Serine, Urea, Sorbitol, Sodium Chloride, Allantoin, Oleyl Alcohol, Ethyl Linoleate.

Doctor Ts Supergoop Broad Spectrum SPF 30+ City Sunscreen Serum 1.7 oz./ 50 ml.

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CITY SUNSCREEN SERUM SPF 30 DOCTOR TS SUPER GOOP
homosalate, octisalate, avobenzene, octocrylene cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:75936-110
Route of Administration	TOPICAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S)	HOMOSALATE	8 g in 100 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4 g in 100 mL
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX)	AVOBENZONE	3 g in 100 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM)	OCTOCRYLENE	2 g in 100 mL

Ingredient Name	Strength
Inactive Ingredients
CYCLOMETHICONE (UNII: NMQ347994Z)
GLYCERIN (UNII: PDC6A3C0OX)
XANTHAN GUM (UNII: TTV12P4NEE)
PANTHENOL (UNII: WV9CM0O67Z)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
POLYOXYL 40 STEARATE (UNII: 13A4J4NH9I)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
SODIUM LACTATE (UNII: TU7HW0W0QT)
LACTIC ACID (UNII: 33X04XA5AT)
SERINE (UNII: 452VLY9402)
UREA (UNII: 8W8T17847W)
SORBITOL (UNII: 506T60A25R)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
ALLANTOIN (UNII: 344S277G0Z)
OLEYL ALCOHOL (UNII: 172F2WN8DV)
ETHYL LINOLEATE (UNII: MJ2YTT4J8M)

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:75936-110-01	50 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product	12/07/2010	07/06/2017

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part352	12/07/2010	07/06/2017

Labeler - Taylor James LLC (033381850)

Registrant - BAXTER LABORATORIES PTY. LTD. (740537709)

Name	Address	ID/FEI	Business Operations
Establishment
BAXTER LABORATORIES PTY. LTD.		740537709	manufacture(75936-110)

Revised: 12/2017

Document Id: e19c3a4b-e6c5-4ab7-be77-8fd9b17dba61

Set id: 8265b0cc-bb38-42db-8719-ea3ed5c118d1

Version: 8

Effective Time: 20171212

Taylor James LLC