TIESO RAPIDO PLUS- homosalate, ethylhexyl salicylate, titanium dioxide, benzalkonium chloride spray

Country: United States

Language: English

Source: NLM (National Library of Medicine)

Active ingredient:

HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S), BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y), TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP), OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W)

Available from:

ATEC CO., LTD.

Administration route:

TOPICAL

Prescription type:

OTC DRUG

Authorization status:

OTC monograph not final

Summary of Product characteristics

TIESO RAPIDO PLUS- HOMOSALATE, ETHYLHEXYL SALICYLATE, TITANIUM
DIOXIDE, BENZALKONIUM
CHLORIDE SPRAY
ATEC CO., LTD.
_Disclaimer: Most OTC drugs are not reviewed and approved by FDA,
however they may be marketed if they_
_comply with applicable regulations and policies. FDA has not
evaluated whether this product complies._
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TIESO RAPIDO PLUS
SUNSCREEN + ANTIBACTERIAL
2.7 FL. OZ. (80 ML)
69978-0081-1
_ACTIVE INGREDIENTS PURPOSES_
Homosalate 5.00 % .......................................... sunscreen
Ethylhexyl Salicylate 4.5% .................................sunscreen
Titanium Dioxide 2.1 % ......................................sunscreen
Benzalkonium Chloride 0.04 % .......................antibacterial
_INACTIVE INGREDIENTS_ Water, Dicaprylyl Carbonate, Alcohol,
Cyclomethicone, Phenylbenzimidazole
Sulfonic Acid, Lepidium Meyenii Root Extract, Glycerin,
1,2-Hexanediol, Bis-Ethylhexyloxyphenol
Methoxyphenyl Triazine, Diethylamino Hydroxybenzoyl Hexyl Benzoate,
C13-16 Isoparaffin, PEG-10
Dimethicone, Sodium Chloride, Heptyl Undecylenate, Sodium Hydroxide,
Aloe Barbadensis Leaf
Extract, Dioscorea Japonica Root Extract, Laminaria Japonica Extract,
Ulmus Davidiana Root Extract,
Viola Mandshurica Flower Extract, Stearic acid, Aluminum Hydroxide,
Butylene Glycol, Disodium
EDTA, Fragrance
TIESO RAPIDO PLUS
homosalate, ethylhexyl salicylate, titanium dioxide, benzalkonium
chloride spray
PRODUCT INFORMATION
PRODUCT T YPE
HUMAN OTC DRUG
ITE M CODE (SOURCE )
NDC:6 9 9 78 -0 0 8 1
ROUTE OF ADMINISTRATION
TOPICAL
ACTIVE INGREDIENT/ACTIVE MOIETY
INGREDIENT NAME
BASIS OF STRENGTH
STRE NG TH
HO MO SALATE (UNII: V0 6 SV4M9 5S) (HOMOSALATE - UNII:V0 6 SV4M9 5S)
HOMOSALATE
4 g in 8 0 mL
BENZALKO NIUM CHLO RIDE (UNII: F5UM2KM3W7) (BENZALKONIUM -
UNII:7N6 JUD5X6 Y)
BENZALKONIUM
CHLORIDE
0 .0 32 g
in 8 0 mL
TITANIUM DIO XIDE (UNII: 15FIX9 V2JP) (TITANIUM DIOXIDE - UNII:15FIX9
V2JP)
TITANIUM DIOXIDE
1.6 8 g in 8 0 mL
O CTISALATE (UNII: 4X49 Y0 59 6 W) (OCTISALATE - UNII:4X49 Y0 59 6 W)
OCTISALATE
3.6 g in 8 0 mL
INACTIVE INGREDIEN