TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 SUNSCREEN- octinoxate, octisalate and zinc oxide lotion 
Allergan, Inc.

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TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 SUNSCREEN- octinoxate, octisalate and zinc oxide lotion 
Allergan, Inc.
Total Defense Repair Broad Spectrum SPF 34 Sunscreen
Drug Facts

Active ingredients

Octinoxate 7.5%

Octisalate 3.0%

Zinc Oxide 8.0%

Purpose

Sunscreen

Sunscreen

Sunscreen

Uses

Warnings

For external use only

Do not use 

on damaged or broken skin

When using this product 

keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor 

if rash occurs

Keep out of reach of children. 

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

Directions

Inactive ingredients

Water, Caprylic/Capric Triglyceride, Silica, Squalane, Glycerin, Niacinamide, Dimethicone, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Butyrospermum Parkii (Shea) Butter, Polygonum Aviculare Extract, Physalis Angulata Extract, Dunaliella Salina Extract, Ubiquinone, Camellia Sinensis Leaf Extract, Tremella Fuciformis Sporocarp Extract, Betaine, Melanin, Tocopheryl Acetate, Tocopherol, Hydroxyacetophenone, Batyl Alcohol, C12-15 Alkyl Benzoate, Panthenol, Butylene Glycol, Ceteareth-20, Polyhydroxystearic Acid, Isostearic Acid, Xanthan Gum, Ethylhexylglycerin, Disodium EDTA, Aminomethyl Propanol, Caprylyl Glycol, Potassium Sorbate, Sorbic Acid, Phenoxyethanol

Other information

Questions or comments

www.skinmedica.com 

Principal Display Panel - Carton Label

TOTAL DEFENSE
+
REPAIR
Broad Spectrum SPF 34 Sunscreen
+ INFRARED PROTECTION
Net Wt. 6 x 1.0 Oz. Travel

TOTAL DEFENSE
+
REPAIR 
Broad Spectrum SPF 34 Sunscreen
+ INFRARED PROTECTION
Net Wt. 6 x 1.0 Oz. Travel

TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 SUNSCREEN 
octinoxate, octisalate and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0023-5494
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE30 mg  in 1 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE80 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
SQUALANE (UNII: GW89575KF9)  
GLYCERIN (UNII: PDC6A3C0OX)  
NIACINAMIDE (UNII: 25X51I8RD4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
SHEA BUTTER (UNII: K49155WL9Y)  
POLYGONUM AVICULARE TOP (UNII: ZCD6009IUF)  
PHYSALIS ANGULATA (UNII: W4TKW9D5GG)  
DUNALIELLA SALINA (UNII: F4O1DKI9A6)  
UBIDECARENONE (UNII: EJ27X76M46)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
TREMELLA FUCIFORMIS FRUITING BODY (UNII: GG8N28393G)  
BETAINE (UNII: 3SCV180C9W)  
MELANIN SYNTHETIC (TYROSINE, PEROXIDE) (UNII: O0CV1RMR44)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TOCOPHEROL (UNII: R0ZB2556P8)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
BATILOL (UNII: 39YR661C4U)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
PANTHENOL (UNII: WV9CM0O67Z)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
ISOSTEARIC ACID (UNII: X33R8U0062)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SORBIC ACID (UNII: X045WJ989B)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0023-5494-231 in 1 CARTON06/15/2015
165 g in 1 TUBE; Type 0: Not a Combination Product
2NDC:0023-5494-011 in 1 CARTON06/15/2015
228.4 g in 1 TUBE; Type 0: Not a Combination Product
3NDC:0023-5494-256 in 1 CARTON06/15/2015
37.08 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02006/15/2015
Labeler - Allergan, Inc. (144796497)

Revised: 9/2015
Document Id: 93ab2b62-c9b0-4ed6-bc97-239cb2a59e12
Set id: 9c9e9d2a-64b1-4b53-81ad-0b347f89a93e
Version: 7
Effective Time: 20150901
 
Allergan, Inc.