DR ZINX MINERAL FACIAL SUNSCREEN FOR DRY SKIN SPF-50- zinc oxide lotion

DR ZINX MINERAL FACIAL SUNSCREEN FOR DRY SKIN by

Drug Labeling and Warnings

DR ZINX MINERAL FACIAL SUNSCREEN FOR DRY SKIN 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

INACTIVE INGREDIENTS

Purified water, Coco-caprylate/caprate, Glycerin, C9-15 alkane, Simmondsia chinensis seed oil (Jojoba), Polyglyceryl-3 Polyricinoleate, Cera alba (Bees Wax), Isostearic acid, Sodium Hyaluronate, Aloe Barbadensis Leaf Extract, Tocopherol (Vitamin E), Polyhydroxystearic acid, Cetyl phosphate, Sodium chloride, Caprylyl glycol, Phenylpropanol, Ethylhexylglycerin Disodium EDTA, Propanediol, Maltodextrin

QUESTIONS OR COMMENTS?

CONTACT@DRZINX.COM

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

DR ZINX MINERAL FACIAL SUNSCREEN FOR DRY SKIN  SPF-50
zinc oxide lotion

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 60396-204
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)
C13-15 ALKANE (UNII: 114P5I43UJ)
JOJOBA OIL (UNII: 724GKU717M)
POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
YELLOW WAX (UNII: 2ZA36H0S2V)
ISOSTEARIC ACID (UNII: X33R8U0062)
HYALURONATE SODIUM (UNII: YSE9PPT4TH)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
TOCOPHEROL (UNII: R0ZB2556P8)
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
CERAMIDE 2 (UNII: C04977SRJ5)
CETYL PHOSPHATE (UNII: VT07D6X67O)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENYLPROPANOL (UNII: 0F897O3O4M)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
EDETATE DISODIUM (UNII: 7FLD91C86K)
PROPANEDIOL (UNII: 5965N8W85T)
MALTODEXTRIN (UNII: 7CVR7L4A2D)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 60396-204-11	50 mL in 1 TUBE; Type 0: Not a Combination Product	05/23/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	05/23/2020

Labeler - ANTARIA PTY LTD (740611405)

Establishment
Name	Address	ID/FEI	Business Operations
ANTARIA PTY LTD		740611405	manufacture(60396-204)