Product NDC: | 10812-972 |
Proprietary Name: | Neutrogena Wet Skin Kids Beach and Pool Sunblock |
Non Proprietary Name: | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Active Ingredient(s): | 30; 150; 50; 100; 30 mg/g; mg/g; mg/g; mg/g; mg/g & nbsp; Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Administration Route(s): | TOPICAL |
Dosage Form(s): | STICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10812-972 |
Labeler Name: | Neutrogena Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111205 |
Package NDC: | 10812-972-01 |
Package Description: | 1 CARTRIDGE in 1 BLISTER PACK (10812-972-01) > 13 g in 1 CARTRIDGE |
NDC Code | 10812-972-01 |
Proprietary Name | Neutrogena Wet Skin Kids Beach and Pool Sunblock |
Package Description | 1 CARTRIDGE in 1 BLISTER PACK (10812-972-01) > 13 g in 1 CARTRIDGE |
Product NDC | 10812-972 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Avobenzone, Homosalate, Octisalate, Octocrylene, and Oxybenzone |
Dosage Form Name | STICK |
Route Name | TOPICAL |
Start Marketing Date | 20111205 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Neutrogena Corporation |
Substance Name | AVOBENZONE; HOMOSALATE; OCTISALATE; OCTOCRYLENE; OXYBENZONE |
Strength Number | 30; 150; 50; 100; 30 |
Strength Unit | mg/g; mg/g; mg/g; mg/g; mg/g |
Pharmaceutical Classes |