NDC 67879-303

SUN THERAPE BODY SPF-35

Homosalate, Octinoxate, Octisalate, Avobenzone

SUN THERAPE BODY SPF-35 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Pharmagel International Inc. The primary component is Homosalate; Octinoxate; Octisalate; Avobenzone.

Product ID67879-303_b1d98f11-0b1a-4cc8-99b2-6e6b5c0fb148
NDC67879-303
Product TypeHuman Otc Drug
Proprietary NameSUN THERAPE BODY SPF-35
Generic NameHomosalate, Octinoxate, Octisalate, Avobenzone
Dosage FormLotion
Route of AdministrationTOPICAL
Marketing Start Date2015-06-18
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart352
Labeler NamePHARMAGEL INTERNATIONAL INC
Substance NameHOMOSALATE; OCTINOXATE; OCTISALATE; AVOBENZONE
Active Ingredient Strength10 g/100mL; g/100mL; g/100mL; g/100mL
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 67879-303-51

1 TUBE in 1 BOX (67879-303-51) > 175 mL in 1 TUBE (67879-303-11)
Marketing Start Date2015-06-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67879-303-11 [67879030311]

SUN THERAPE BODY SPF-35 LOTION
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-18

NDC 67879-303-51 [67879030351]

SUN THERAPE BODY SPF-35 LOTION
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2015-06-18

Drug Details

Active Ingredients

IngredientStrength
HOMOSALATE10 g/100mL

OpenFDA Data

SPL SET ID:2da3a65a-59c1-4f96-9be6-c4ace54597b2
Manufacturer
UNII

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