NDC 50260-800

Lip Balm SPF 15

Octinoxate Oxybenzone

Lip Balm SPF 15 is a Topical Ointment in the Human Otc Drug category. It is labeled and distributed by Fercy Personal Care Products Co Limited. The primary component is Oxybenzone; Octinoxate.

Product ID50260-800_6033f19a-bfc6-494f-89ca-efb8b0a7ed8d
NDC50260-800
Product TypeHuman Otc Drug
Proprietary NameLip Balm SPF 15
Generic NameOctinoxate Oxybenzone
Dosage FormOintment
Route of AdministrationTOPICAL
Marketing Start Date2010-12-09
Marketing CategoryOTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
Application Numberpart352
Labeler NameFercy Personal Care Products Co Limited
Substance NameOXYBENZONE; OCTINOXATE
Active Ingredient Strength3 g/100g; g/100g
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 50260-800-08

8 g in 1 TUBE (50260-800-08)
Marketing Start Date2010-12-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50260-800-05 [50260080005]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-06 [50260080006]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-04 [50260080004]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-03 [50260080003]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-07 [50260080007]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-08 [50260080008]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-02 [50260080002]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-09 [50260080009]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

NDC 50260-800-01 [50260080001]

Lip Balm SPF 15 OINTMENT
Marketing CategoryOTC monograph final
Application Numberpart352
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-12-09
Inactivation Date2019-10-29

Drug Details

Active Ingredients

IngredientStrength
OXYBENZONE3 g/100g

OpenFDA Data

SPL SET ID:6142b334-f766-46d0-91ab-1bccb78c3946
Manufacturer
UNII

NDC Crossover Matching brand name "Lip Balm SPF 15" or generic name "Octinoxate Oxybenzone"

NDCBrand NameGeneric Name
50260-800Lip Balm SPF 15Octinoxate OXYBENZONE
76354-110LIP BALM SPF 15LIP BALM SPF 15
65692-1006Bullet LineLip Balm SPF 15
65692-1007Bullet LineLip Balm SPF 15
65692-1008Bullet LineLip Balm SPF 15
65692-1009Bullet LineLip Balm SPF 15
65692-1010Bullet LineLip Balm SPF 15
65692-1011Bullet LineLip Balm SPF 15
65692-1012Bullet LineLip Balm SPF 15
55301-002Exchange Select Sport SunscreenOCTINOXATE OXYBENZONE
55301-003Exchange Select Sport SunscreenOCTINOXATE OXYBENZONE
55301-000Exchange Select SunscreenOCTINOXATE OXYBENZONE
55301-001Exchange Select SunscreenOCTINOXATE OXYBENZONE
30142-925Kroger SunscreenOCTINOXATE OXYBENZONE
0363-4001Walgreens SunscreenOCTINOXATE OXYBENZONE
0363-4005Walgreens Sunscreen SportOCTINOXATE OXYBENZONE
12027-100wet n wildOCTINOXATE OXYBENZONE
12027-102wet n wildOCTINOXATE OXYBENZONE
12027-103wet n wildOCTINOXATE OXYBENZONE
12027-104wet n wildOCTINOXATE OXYBENZONE

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