ETADERM TATTOO SUNSCREEN BROAD SPECTRUM SPF-30- zinc oxide cream 
NUEPHASE LLC

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ETADERM Tattoo Sunscreen Broad Spectrum SPF-30

Drug Facts

Active Ingredients

Zinc Oxide 15.00%

Purpose

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 or irritation develops and lasts.

Keep out of reach of children.

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

If pregnant or breast-feeding, 

ask a health professional before use

Directions:

Other Information:

Inactive Ingredients:

Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Argania Spinosa (Argan) Oil, Ascorbic Acid (Vitamin E), Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Calendula Officinalis Extract, Caprylic/Capric Triglyceride, Caprylyl Glycol, Cetearyl Olivate, Cetyl Alcohol, Chamomilla Matricaria (Chamomile) Extract, Citric Acid, Cucumis Sativus (Cucumber) Extract, Daucus Carota Sativa (Carrot) Extract, Glycerin, Glyceryl Laurate, Glyceryl Stearate, Glyceryl Undecylenate, Helianthus Annuus (Sun flower) Oil, Hydrolyzed Collagen, Polyhydroxy stearic Acid, Polysorbate 20, Rosa Canina (Rose) Hips Oil, Sorbitan Olivate, Theobroma Cacao (Cocoa)Butter, Tocopheryl Acetate (Vitamin E), Xanthan Gum, Zemea (Corn) Propanediol

Questions?

Please visit our website, www.etaderm.com

Package Labeling:

Bottle

ETADERM TATTOO SUNSCREEN BROAD SPECTRUM SPF-30 
zinc oxide cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84180-472
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION150 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
WATER (UNII: 059QF0KO0R)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)  
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
CETEARYL OLIVATE (UNII: 58B69Q84JO)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
CHAMOMILE (UNII: FGL3685T2X)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
CUCUMBER (UNII: YY7C30VXJT)  
CARROT (UNII: L56Z1JK48B)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL LAURATE (UNII: Y98611C087)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
SORBITAN OLIVATE (UNII: MDL271E3GR)  
COCOA (UNII: D9108TZ9KG)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
XANTHAN GUM (UNII: TTV12P4NEE)  
CORN (UNII: 0N8672707O)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84180-472-00118 mL in 1 BOTTLE; Type 0: Not a Combination Product04/01/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02004/01/2024
Labeler - NUEPHASE LLC (118900101)

Revised: 3/2024
Document Id: 1414184a-a7b6-ff46-e063-6394a90a932b
Set id: cc1e3485-57e6-4ac9-96b3-2d683beb5b53
Version: 1
Effective Time: 20240320
 
NUEPHASE LLC