DR ZINX BRIGHTENING MINERAL SUNSCREEN SPF-50- zinc oxide lotion

DR ZINX BRIGHTENING MINERAL SUNSCREEN by

Drug Labeling and Warnings

DR ZINX BRIGHTENING MINERAL SUNSCREEN by is a Otc medication manufactured, distributed, or labeled by ANTARIA PTY LTD. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ZINC OXIDE (25.0% W/W)

PURPOSE

SUNSCREEN

USES

• Helps prevent sunburn
• If used as directed with other sun protection measures (see Directions), decreased the risk of skin cancer and early skin aging caused by the sun

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 doctor if rash occurs

DIRECTIONS

apply liberally and evenly 20 minutes before sun exposure
reapply:

•      After 40 minutes of swimming or sweating
•      Immediately after towel drying
•      at least every 2 hours

Sun Protection Measures: Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:
   limit time in the sun, especially from 10 a.m. – 2 p.m.
   wear long-sleeved shirts, pants, hats, and sunglasses
children under 6 months of age: ask a doctor

OTHER INFORMATION

Store at temperatures below 90°F (30°C). Protect the product in this container from expressive heat and direct sun.

INACTIVE INGREDIENTS

Demineralised water, Coco-Caprylate/Caprate, Glycerine, C12-C19 Alkane, Simmondia Chinesis (Jojoba) Seed Oil, Polyglyceryl -3-Polyricinoleate, Citrus Unshiu Peel Extract, Cera Alba, Isotearic Acid, Polyhydroxystearic Acid, Maltodextrin, Tocopherol, Caprylyl Glycol, Propanediol, Cetyl Phosphate, Sodium Choride, Disodium EDTA, Ethylhexylglycerin

QUESTIONS?

CONTACT@DRZINX.COM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR ZINX BRIGHTENING MINERAL SUNSCREEN  SPF-50
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60396-212
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	25 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
GLYCERIN (UNII: PDC6A3C0OX)
COCONUT ALKANES (UNII: 1E5KJY107T)
JOJOBA OIL (UNII: 724GKU717M)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
TANGERINE PEEL (UNII: JU3D414057)
YELLOW WAX (UNII: 2ZA36H0S2V)
ISOSTEARIC ACID (UNII: X33R8U0062)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
MALTODEXTRIN (UNII: 7CVR7L4A2D)
TOCOPHEROL (UNII: R0ZB2556P8)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PROPANEDIOL (UNII: 5965N8W85T)
CETYL PHOSPHATE (UNII: VT07D6X67O)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60396-212-11	50 mL in 1 TUBE; Type 0: Not a Combination Product	05/28/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/28/2020

Labeler - ANTARIA PTY LTD (740611405)

Establishment
Name	Address	ID/FEI	Business Operations
ANTARIA PTY LTD		740611405	manufacture(60396-212)