NDC 71702-110

CLEMATIS Morning Dew CC

Octinoxate, Titanium Dioxide, Octisalate, Homosalate

CLEMATIS Morning Dew CC is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Coshub Co., Ltd.. The primary component is Octinoxate; Titanium Dioxide; Octisalate; Homosalate.

Product ID71702-110_9d2c27ed-d394-4764-86fd-a3d2293a68e8
NDC71702-110
Product TypeHuman Otc Drug
Proprietary NameCLEMATIS Morning Dew CC
Generic NameOctinoxate, Titanium Dioxide, Octisalate, Homosalate
Dosage FormCream
Route of AdministrationTOPICAL
Marketing Start Date2017-08-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameCoshub Co., Ltd.
Substance NameOCTINOXATE; TITANIUM DIOXIDE; OCTISALATE; HOMOSALATE
Active Ingredient Strength4 g/50mL; g/50mL; g/50mL; g/50mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 71702-110-02

1 TUBE in 1 CARTON (71702-110-02) > 50 mL in 1 TUBE (71702-110-01)
Marketing Start Date2017-08-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71702-110-02 [71702011002]

CLEMATIS Morning Dew CC CREAM
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-01

NDC 71702-110-01 [71702011001]

CLEMATIS Morning Dew CC CREAM
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-08-01

Drug Details

Active Ingredients

IngredientStrength
OCTINOXATE3.5 g/50mL

OpenFDA Data

SPL SET ID:655d52ed-976c-4f22-94c4-667a188012b2
Manufacturer
UNII

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