NDC 58418-001

SS-TMPFL

Bs Spf30 Spray - Dl

SS-TMPFL is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Tropical Enterprises International, Inc.. The primary component is Octocrylene; Avobenzone.

Product ID58418-001_092e4d2e-8fb8-34d7-e054-00144ff88e88
NDC58418-001
Product TypeHuman Otc Drug
Proprietary NameSS-TMPFL
Generic NameBs Spf30 Spray - Dl
Dosage FormSpray
Route of AdministrationTOPICAL
Marketing Start Date2018-10-01
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameTropical Enterprises International, Inc.
Substance NameOCTOCRYLENE; AVOBENZONE
Active Ingredient Strength8 mg/mL; mg/mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 58418-001-01

30 mL in 1 BOTTLE, DISPENSING (58418-001-01)
Marketing Start Date2018-10-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58418-001-28 [58418000128]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-04 [58418000104]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-70 [58418000170]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01

NDC 58418-001-64 [58418000164]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-08 [58418000108]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-16 [58418000116]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-02 [58418000102]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-32 [58418000132]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01

NDC 58418-001-12 [58418000112]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-10 [58418000110]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

NDC 58418-001-01 [58418000101]

SS-TMPFL SPRAY
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-10-01
Inactivation Date2020-01-31
Reactivation Date2020-02-03

Drug Details

Active Ingredients

IngredientStrength
OCTOCRYLENE8 mg/mL

OpenFDA Data

SPL SET ID:70ac6e5f-2fca-733a-e053-2a91aa0aaf5b
Manufacturer
UNII

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