ELROEL PANG PANG SUN CUSHION S7- zinc oxide, titanium dioxide, octinoxate, octisalate cream

ELROEL Pang Pang Sun Cushion S7 by

Drug Labeling and Warnings

ELROEL Pang Pang Sun Cushion S7 by is a Otc medication manufactured, distributed, or labeled by MONOGLOT HOLDINGS Inc., Cit Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ZINC OXIDE 9.70%

OCTINOXATE 7.00%
OCTISALATE 3.00%

TITANIUM DIOXIDE 1.52%

PURPOSE

Sunscreen

INDICATIONS & USAGE

Helps prevent sunburn

DOSAGE & ADMINISTRATION

For sunscreen use:
■ apply liberally 15 minutes before sun exposure
■ reapply at least every two hours
■ use a water resistant sunscreen if swimming or sweating
■ 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

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 using and ask a doctor if rash occurs.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT

Aloe Barbadensis Leaf JuiceCyclopentasiloxane, Butylene Glycol, Butyloctyl Salicylate, Caprylyl Methicone, Diethylamino Hydroxybenzoyl Hexyl Benzoate, Cetyl PEG/PPG-10/1 Dimethicone, Cyclohexasiloxane, Niacinamide, Diphenylsiloxy Phenyl Trimethicone, Alcohol Denat., Propylene Glycol Dicaprylate, Sodium Chloride, Silica, Vinyl Dimethicone/Methicone Silsesquioxane Crosspolymer, Hydroxyacetophenone, Synthetic Beeswax, Disteardimonium Hectorite, Triethoxycaprylylsilane, Dipropylene Glycol, Water, Fragrance, Caprylyl Glycol, Squalane, Tocopheryl Acetate, Propylene Carbonate, Ethylhexylglycerin, Glycerin, Adenosine, Butyrospermum Parkii (Shea) Butter, Xylitylglucoside, Anhydroxylitol, Disodium EDTA, Methyl Diisopropyl Propionamide, Laminaria Japonica Extract, Ulmus Davidiana Root Extract, Aloe Barbadensis Leaf Extract, Viola Mandshurica Flower Extract, Dioscorea Japonica Root Extract, Xylitol, CI 77492, 1,2-Hexanediol, Glucose, Menthyl Lactate, Beeswax, Ethyl Menthane Carboxamide, Glyceryl Stearate, Caprylic/Capric Triglyceride, Hydrogenated Phosphatidylcholine, Calcium Pantothenate, Centella Asiatica Extract, Sucrose Stearate, Stearamidopropyl Dimethylamine Lactate, Phenethyl Alcohol, PEG-100 Stearate, Sodium Ascorbyl Phosphate, Dipotassium Glycyrrhizate, Cetearyl Alcohol, Polyquaternium-67, Pyridoxine HCl, Madecassoside, Madecassic Acid, Asiaticoside, Asiatic Acid

OTHER SAFETY INFORMATION

Protect the product in this container from excessive heat and direct sunlight

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ELROEL PANG PANG SUN CUSHION S7 
zinc oxide, titanium dioxide, octinoxate, octisalate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83154-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP)	TITANIUM DIOXIDE	1.52 g  in 100 g
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37)	ZINC CATION	9.7 g  in 100 g
OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51)	OCTINOXATE	7 g  in 100 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)	OCTISALATE	3 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)
DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
DIPROPYLENE GLYCOL (UNII: E107L85C40)
WATER (UNII: 059QF0KO0R)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
SQUALANE (UNII: GW89575KF9)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
ALUMINUM OXIDE (UNII: LMI26O6933)
GLYCERIN (UNII: PDC6A3C0OX)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SHEA BUTTER (UNII: K49155WL9Y)
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
ADENOSINE (UNII: K72T3FS567)
XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
ANHYDROXYLITOL (UNII: 8XWR7NN42F)
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
METHYL DIISOPROPYL PROPIONAMIDE (UNII: 6QOP5A9489)
LAMINARIA JAPONICA (UNII: WE98HW412B)
ULMUS DAVIDIANA ROOT (UNII: URQ79U8261)
VIOLA MANDSHURICA FLOWER (UNII: 46MR945M6X)
DIOSCOREA JAPONICA TUBER (UNII: I43FCF3356)
XYLITOL (UNII: VCQ006KQ1E)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
1,2-HEXANEDIOL (UNII: TR046Y3K1G)
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)
YELLOW WAX (UNII: 2ZA36H0S2V)
ETHYL MENTHANE CARBOXAMIDE (UNII: 6S7S02945H)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
CALCIUM PANTOTHENATE (UNII: 568ET80C3D)
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
SUCROSE STEARATE (UNII: 274KW0O50M)
STEARAMIDOPROPYL DIMETHYLAMINE LACTATE (UNII: 31Q9363QSX)
PHENYLETHYL ALCOHOL (UNII: ML9LGA7468)
PEG-100 STEARATE (UNII: YD01N1999R)
SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
MADECASSOSIDE (UNII: CQ2F5O6YIY)
MADECASSIC ACID (UNII: M7O1N24J82)
ASIATICOSIDE (UNII: PKO39VY215)
ASIATIC ACID (UNII: 9PA5A687X5)
ALOE VERA LEAF (UNII: ZY81Z83H0X)
CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
AMILOXATE (UNII: 376KTP06K8)
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
DIETHYLAMINO HYDROXYBENZOYL HEXYL BENZOATE (UNII: ANQ870JD20)
CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)
CYCLOMETHICONE 6 (UNII: XHK3U310BA)
NIACINAMIDE (UNII: 25X51I8RD4)
DIPHENYLSILOXY PHENYL TRIMETHICONE (UNII: I445L28B12)
ALCOHOL (UNII: 3K9958V90M)
PROPYLENE GLYCOL DICAPRYLATE (UNII: 581437HWX2)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83154-003-02	1 in 1 CARTON	02/03/2024
1	NDC: 83154-003-01	25 g in 1 CONTAINER; Type 0: Not a Combination Product
2	NDC: 83154-003-04	1 in 1 CARTON	02/03/2024
2	NDC: 83154-003-03	8 g in 1 CONTAINER; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	02/03/2024

Labeler - MONOGLOT HOLDINGS Inc. (694628175)

Registrant - MONOGLOT HOLDINGS Inc. (694628175)

Establishment
Name	Address	ID/FEI	Business Operations
Cit Co., Ltd.		690081646	manufacture(83154-003)