CoreTex Sun X SPF 30 is a Topical Lotion in the Human Otc Drug category. It is labeled and distributed by Coretex Products. The primary component is Avobenzone; Homosalate; Octinoxate; Octisalate; Oxybenzone.
Product ID | 65753-100_5ef74e6a-52ae-46e9-e053-2991aa0a53e4 |
NDC | 65753-100 |
Product Type | Human Otc Drug |
Proprietary Name | CoreTex Sun X SPF 30 |
Generic Name | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
Dosage Form | Lotion |
Route of Administration | TOPICAL |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL |
Application Number | part352 |
Labeler Name | CoreTex Products |
Substance Name | AVOBENZONE; HOMOSALATE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Active Ingredient Strength | 1 g/100mL; g/100mL; g/100mL; g/100mL; g/100mL |
NDC Exclude Flag | E |
Listing Certified Through | 2018-12-31 |
Marketing Start Date | 2019-11-26 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-01-01 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2017-11-27 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2019-11-26 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Marketing Category | OTC monograph not final |
Application Number | part352 |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 2013-01-25 |
Ingredient | Strength |
---|---|
AVOBENZONE | 1 g/100mL |
SPL SET ID: | 9a120b1e-f932-43c7-9a65-ef25407a677a |
Manufacturer | |
UNII |
NDC | Brand Name | Generic Name |
---|---|---|
65753-100 | CoreTex Sun X SPF 30 | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
65753-101 | CoreTex Sun X SPF 30 Thin | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
69842-118 | CVS Health | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
63940-065 | HARMON FACE VALUES ULTRA LIGHT DRY TO THE TOUCH SPF 30 SUNSCREEN | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
51531-0349 | Mary Kay Suncare Sunscreen SPF 30 | avobenzone, homosalate, octinoxate, octisalate, oxybenzone |
70381-104 | MURAD - AGE REFORM - PERFECTING DAY | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
70381-105 | MURAD - AGE REFORM - PERFECTING DAY | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
70381-103 | MURAD - ENVIRONMENTAL SHIELD - ESSENTIAL-C DAY MOISTURE BROAD SPECTRUM | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
65753-103 | Rainbow Broad Spectrum SPF 30 | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
53634-255 | SPF 30 face Moisturizer | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
65753-102 | Sun X Multi-Pack SPF 30 Thick | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
14743-536 | Tahitian Noni | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
44717-536 | Tahitian Noni | Avobenzone, Homosalate, Octinoxate, Octisalate, Oxybenzone |
67038-110 | THE YOUTH AS WE KNOW IT | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
49893-300 | Total Suncare Sunscreen SPF 50 | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
49893-500 | Total Suncare Sunscreen SPF 70 | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |
0363-0940 | WALGREENS BROAD SPECTRUM SPF 30 DRY TOUCH SUNSCREEN | AVOBENZONE, HOMOSALATE, OCTINOXATE, OCTISALATE, OXYBENZONE |