NDC 71011-002

sunscreen lip balm

Padimate O,octinoxate

sunscreen lip balm is a Topical Stick in the Human Otc Drug category. It is labeled and distributed by Ningbo Huize Commodity Co.,ltd.. The primary component is Octinoxate; Padimate O.

Product ID71011-002_621702a3-9d4f-4663-e053-2991aa0a5f38
NDC71011-002
Product TypeHuman Otc Drug
Proprietary Namesunscreen lip balm
Generic NamePadimate O,octinoxate
Dosage FormStick
Route of AdministrationTOPICAL
Marketing Start Date2016-10-08
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart352
Labeler NameNingBo Huize Commodity Co.,Ltd.
Substance NameOCTINOXATE; PADIMATE O
Active Ingredient Strength4 g/100g; g/100g
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 71011-002-02

13 g in 1 PACKAGE (71011-002-02)
Marketing Start Date2016-10-20
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71011-002-01 [71011000201]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-05 [71011000205]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-06 [71011000206]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-11 [71011000211]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-12 [71011000212]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-02 [71011000202]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-15 [71011000215]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-04 [71011000204]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-16 [71011000216]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-08 [71011000208]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-13 [71011000213]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-07 [71011000207]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-17 [71011000217]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-09 [71011000209]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-03 [71011000203]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

NDC 71011-002-14 [71011000214]

sunscreen lip balm STICK
Marketing CategoryOTC monograph not final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-10-20
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
OCTINOXATE4 g/100g

OpenFDA Data

SPL SET ID:3f42326a-6b33-31eb-e054-00144ff88e88
Manufacturer
UNII

NDC Crossover Matching brand name "sunscreen lip balm" or generic name "Padimate O,octinoxate"

NDCBrand NameGeneric Name
71011-002sunscreen lip balmPADIMATE O,OCTINOXATE
62932-177LIP BALMSUNSCREEN LIP BALM
62932-186LIP BALMSUNSCREEN LIP BALM
62932-236LIP BALMSUNSCREEN LIP BALM
62932-237LIP BALMSUNSCREEN LIP BALM

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.