LA DEFENSE BROAD SPECTRUM SPF 30 MINERAL SUNSCREEN- zinc oxide lotion 
Luzern Laboratories, Inc

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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La Defense
Broad Spectrum SPF 30
Mineral Sunscreen

Active Ingredients

Zinc Oxide (CI 77947) 15%

Purpose

Sunscreen

Uses

Helps prevent sunburn

Warnings

For external use only. Avoid contact with eyes. If contact occurs, rinse thoroughly with water. Discontinue use if skin irritation develops or increases. If irritation persists, consult a health care practitioner.

Keep out of reach of children.

Consult a health care practitioner prior to use on children less than six months of age.

Directions

Apply liberally before sun exposure. Reapply every 2 hours of sun exposure, or after swimming, excessive perspiration, or towel drying.

INACTIVE INGREDIENTS:

ALGAE EXTRACT*†, BUDDLEJA DAVIDII EXTRACT**†, C12-20 ALKYL GLUCOSIDE*†, C14-22 ALCOHOLS*†, CAPRYLHYDROXAMIC ACID*†, CAMELLIA SINENSIS (GREEN TEA) LEAF EXTRACT**†, CAPRYLIC/CAPRIC TRIGLYCERIDE*†, CARBOMER†, CETYL ALCOHOL*†, CITRIC ACID*†, CUCUMIS SATIVUS (CUCUMBER) OIL**†, CYCLOMETHICONE†, ETHYLHEXYL ISONONANOATE†, ETHYLHEXYLGLYCERIN*†, GLYCERIN**†, GLYCERYL CAPRYLATE*†, GLYCERYL UNDECYLENATE*†, GLYCYRRHIZA GLABRA (LICORICE) ROOT EXTRACT**†, HEXYLDECANOL*†, ISOSTEARYL PALMITATE*†, L-ARGININE*†, LEONTOPDOIUM ALPINUM (EDELWEISS) EXTRACT**†, METHYLCELLULOSE*†, METHYLPROPANEDIOL†, OCTYLDODECYL NEOPENTANOATE†, PANTHENOL*†, PROPANEDIOL*†, SODIUM ASCORBYL PHOSPHATE*†, SODIUM HYALURONATE*†, SODIUM PCA*†, STEARETH-2, STEARETH-21, TETRASODIUM GLUTAMATE DIACETATE*†, THYMUS VULGARIS (THYME) EXTRACT**†, TOCOPHERSOLAN†, TOCOPHERYL ACETATE*†, WATER (AQUA)*†, ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT**†.

*NATURAL-DERIVED / DÉRIVÉS DE NATUREL AND/OR ECOCERT
**CERTIFIED ORGANIC/CERTIFIÉ ORGANIQUE USDA/ECOCERT/BIO-SUISSE
† ENVIRONMENTAL WORKING GROUP (EWG) LOW HAZARD RATING OF “GREEN 0 – 2” (NON-TOXIC, NON-IRRITATING)

Principal Display Panel - Carton Label

LA DEFENSE

BROAD SPECTRUM SPF 30
MINERAL SUNSCREEN

LARGE SPECTRE SPF 30
PROTECTION SOLAIRE MINÉRALE

LUZERN®
LABORATORIES

ALL SKIN TYPES • TOUS TYPES DE PEAU

1.7 FL OZ / 50 ml

Carton Label.jpg
LA DEFENSE BROAD SPECTRUM SPF 30 MINERAL SUNSCREEN 
zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63127-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE15 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
BUDDLEJA DAVIDII LEAF (UNII: X380815D32)  
C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)  
C14-22 ALCOHOLS (UNII: B1K89384RJ)  
CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)  
GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)  
HEXYLDECANOL (UNII: 151Z7P1317)  
ISOSTEARYL PALMITATE (UNII: 9EHU0R7ER1)  
ARGININE (UNII: 94ZLA3W45F)  
LEONTOPODIUM NIVALE SUBSP. ALPINUM ROOT (UNII: SDW6SS1K6I)  
METHYLPROPANEDIOL (UNII: N8F53B3R4R)  
OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
PANTHENOL (UNII: WV9CM0O67Z)  
PROPANEDIOL (UNII: 5965N8W85T)  
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
STEARETH-2 (UNII: V56DFE46J5)  
STEARETH-21 (UNII: 53J3F32P58)  
TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)  
THYME (UNII: CW657OBU4N)  
TOCOPHERSOLAN (UNII: O03S90U1F2)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
WATER (UNII: 059QF0KO0R)  
GINGER (UNII: C5529G5JPQ)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63127-100-011 in 1 CARTON03/13/201409/30/2020
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35203/13/201409/30/2020
Labeler - Luzern Laboratories, Inc (188040476)
Establishment
NameAddressID/FEIBusiness Operations
Fragrance Manufacturing, Inc.793406000MANUFACTURE(63127-100)

Revised: 12/2021
 
Luzern Laboratories, Inc