Product NDC: | 75866-301 |
Proprietary Name: | Bubble Gum Sunscreen Lip Moisturizer |
Non Proprietary Name: | OCTINOXATE, OXYBENZONE |
Active Ingredient(s): | 7; 3 g/100g; g/100g & nbsp; OCTINOXATE, OXYBENZONE |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIPSTICK |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75866-301 |
Labeler Name: | Beacon Promotions |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part352 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20101229 |
Package NDC: | 75866-301-01 |
Package Description: | 4.2 g in 1 CONTAINER (75866-301-01) |
NDC Code | 75866-301-01 |
Proprietary Name | Bubble Gum Sunscreen Lip Moisturizer |
Package Description | 4.2 g in 1 CONTAINER (75866-301-01) |
Product NDC | 75866-301 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | OCTINOXATE, OXYBENZONE |
Dosage Form Name | LIPSTICK |
Route Name | TOPICAL |
Start Marketing Date | 20101229 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Beacon Promotions |
Substance Name | OCTINOXATE; OXYBENZONE |
Strength Number | 7; 3 |
Strength Unit | g/100g; g/100g |
Pharmaceutical Classes |