POST RAYS BLEMISH BALM- zinc oxide, titanium dioxide, octinoxate cream

Post rays Blemish Balm by

Drug Labeling and Warnings

Post rays Blemish Balm by is a Otc medication manufactured, distributed, or labeled by Humex,Inc, HANACOS CO., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts Active Ingredient Purpose

Zinc Oxide (3.5%)--------------------------Sunscreen

Titanium Dioxide (5.99%)---------------Sunscreen

Octinoxate (6.5%)-------------------------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

▪ Appy 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, Cetyl Ethylhexanoate, Propylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Isononyl Isononanoate, Clydomethicones, Sorbitan Sesquioleate, Talc, Mineral Oil, Arbutin, Medium-Chain Triglyceride, Microcrystalline Wax, Magnesium Sulfate, Dimethicone, Bentoquatam, Methyl Methacrylate/Glycol Dimethacrylate Crosspolymer, Phenoxyethanol, Ferric Oxide Yellow, Ferrosoferric Oxide, Ferric Oxide Red, Aluminum Hydroxide, PEG-10 Dimethicone Crosspolymer, Triethoxycaprylylsilane, Allantoin, Adenosine, Purslane, Aloe Vera Leaf, Chamaemelum Nobile Flower, Hyaluronate Sodium

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

POST RAYS BLEMISH BALM 
zinc oxide, titanium dioxide, octinoxate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 76344-8003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	5.98878 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	6.5 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z)	ZINC OXIDE	3.5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)	0.5 g  in 100 g
FERROSOFERRIC OXIDE (UNII: XM0M87F357)	0.29792 g  in 100 g
FERRIC OXIDE RED (UNII: 1K09F3G675)	0.25872 g  in 100 g
CETYL ETHYLHEXANOATE (UNII: 134647WMX4)	7 g  in 100 g
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)	0.1482 g  in 100 g
ALLANTOIN (UNII: 344S277G0Z)	0.1 g  in 100 g
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)	0.3136 g  in 100 g
DIMETHICONE (UNII: 92RU3N3Y1O)	0.95 g  in 100 g
ADENOSINE (UNII: K72T3FS567)	0.04 g  in 100 g
ALOE VERA LEAF (UNII: ZY81Z83H0X)	0.01 g  in 100 g
HYALURONATE SODIUM (UNII: YSE9PPT4TH)	0.00005 g  in 100 g
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)	6 g  in 100 g
PURSLANE (UNII: M6S840WXG5)	0.01 g  in 100 g
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)	0.01 g  in 100 g
ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)	0.18522 g  in 100 g
TALC (UNII: 7SEV7J4R1U)	2.21756 g  in 100 g
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 5) (UNII: 035JKJ76MT)	3 g  in 100 g
ARBUTIN (UNII: C5INA23HXF)	2 g  in 100 g
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)	1.8 g  in 100 g
MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)	1.5 g  in 100 g
MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)	1 g  in 100 g
PHENOXYETHANOL (UNII: HIE492ZZ3T)	0.40003 g  in 100 g
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)	2.5 g  in 100 g
MINERAL OIL (UNII: T5L8T28FGP)	2 g  in 100 g
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)	2.9 g  in 100 g
ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)	3 g  in 100 g
BENTOQUATAM (UNII: 7F465U79Q1)	0.8 g  in 100 g

Product Characteristics
Color	brown (Yellowish Brown)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 76344-8003-2	1 in 1 BOX	12/01/2019
1	NDC: 76344-8003-1	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
HANACOS CO., LTD.		690177857	manufacture(76344-8003)