POST RAYS UV PROTECT SUN BLOCK- zinc oxide,octinoxate, octisalate,titamium dioxide cream

Post Rays UV Protect Sun Block by

Drug Labeling and Warnings

Post Rays UV Protect Sun Block by is a Otc medication manufactured, distributed, or labeled by Humex,Inc, Kolmar Korea. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredient Purpose

Zinc Oxide (5.006%)-----------------------------Sunscreen
Octinoxate (6.8%)--------------------------------Sunscreen
Octisalate (4%)------------------------------------Sunscreen
Titanium Dioxide (4.0014%)-------------------Sunscreen

Uses

Helps prevent sunburn

Warnings

Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

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 swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

▪ Apply liberally 15 minutes before sun exposure
▪ Reapply at least every 2 hours
▪ Use a water-resistant sunscreen if swimming or sweating
▪ Children under 6 months of age: ask a doctor

Other Information

▪ protect the product in this container from excessive heat and direct sun

Inactive Ingredients

water, cyclomethicone, methicone, aluminum hydroxide,dimethicone, dipropylene glycol, peg-10 dimethicone, glycerin, dicaprylyl carbonate, propanediol, saccharide hydrolysate(invert sugar), 1,2-hexandediol, salvia hispanica seed (chia seed) extract, curcuma longa (turmeric) root extract, caprylyl trisiloxane, disteardimonium hectorite, magnesium sulfate, dimethicone/vinyl dimethicone crosspolymer, caprylyl glycol, ethylhexylglycerin, glyceryl monocaprylate

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POST RAYS UV PROTECT SUN BLOCK 
zinc oxide,octinoxate, octisalate,titamium dioxide cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76344-8002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	4.0014 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	5.006 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6.8 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	4.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
DIMETHICONE (UNII: 92RU3N3Y1O)	0.2565 g  in 100 g
GLYCERIN (UNII: PDC6A3C0OX)	2 g  in 100 g
DIPROPYLENE GLYCOL (UNII: E107L85C40)	3 g  in 100 g
INVERT SUGAR (UNII: ED959S6ACY)	0.1 g  in 100 g
SALVIA HISPANICA SEED (UNII: NU0OLX06F8)	0.01 g  in 100 g
CAPRYLYL GLYCOL (UNII: 00YIU5438U)	0.2 g  in 100 g
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)	0.5643 g  in 100 g
PROPANEDIOL (UNII: 5965N8W85T)	0.1 g  in 100 g
1,2-HEXANEDIOL (UNII: TR046Y3K1G)	0.02 g  in 100 g
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)	2 g  in 100 g
METHICONE (20 CST) (UNII: 6777U11MKT)	0.2084 g  in 100 g
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)	1 g  in 100 g
MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)	0.8 g  in 100 g
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)	0.8 g  in 100 g
TURMERIC (UNII: 856YO1Z64F)	0.01 g  in 100 g
GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)	0.1 g  in 100 g
PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)	3 g  in 100 g
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)	0.1 g  in 100 g
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)	13 g  in 100 g

Product Characteristics
Color	white (Milky White)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76344-8002-2	1 in 1 BOX	12/01/2019
1	NDC: 76344-8002-1	50 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part352	12/01/2019

Labeler - Humex,Inc (017945311)

Establishment
Name	Address	ID/FEI	Business Operations
HNG		689851457	manufacture(76344-8002)