Product NDC: | 31190-700 |
Proprietary Name: | SunScreen SPF 30 |
Non Proprietary Name: | AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
Active Ingredient(s): | 2; 7.5; 5; 6 g/100g; g/100g; g/100g; g/100g & nbsp; AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 31190-700 |
Labeler Name: | Shanghai Kejing Cleaning Products Co., Ltd. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110901 |
Package NDC: | 31190-700-17 |
Package Description: | 1 TUBE in 1 CARTON (31190-700-17) > 17 g in 1 TUBE |
NDC Code | 31190-700-17 |
Proprietary Name | SunScreen SPF 30 |
Package Description | 1 TUBE in 1 CARTON (31190-700-17) > 17 g in 1 TUBE |
Product NDC | 31190-700 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | AVOBENZONE,OCTINOXATE, OCTISALATE, OXYBENZONE |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20110901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Shanghai Kejing Cleaning Products Co., Ltd. |
Substance Name | AVOBENZONE; OCTINOXATE; OCTISALATE; OXYBENZONE |
Strength Number | 2; 7.5; 5; 6 |
Strength Unit | g/100g; g/100g; g/100g; g/100g |
Pharmaceutical Classes |