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Vanilla Sunscreen Lip Moisturizer
Vanilla Sunscreen Lip Moisturizer - 75866-307-01 - (OCTINOXATE, OXYBENZONE)
Drug Information of Vanilla Sunscreen Lip Moisturizer
| Product NDC: | 75866-307 |
| Proprietary Name: | Vanilla 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) |
Labeler Information of Vanilla Sunscreen Lip Moisturizer
| Product NDC: | 75866-307 |
| Labeler Name: | Beacon Promotions, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20101229 |
Package Information of Vanilla Sunscreen Lip Moisturizer
| Package NDC: | 75866-307-01 |
| Package Description: | 4.2 g in 1 CONTAINER (75866-307-01) |
NDC Information of Vanilla Sunscreen Lip Moisturizer
| NDC Code | 75866-307-01 |
| Proprietary Name | Vanilla Sunscreen Lip Moisturizer |
| Package Description | 4.2 g in 1 CONTAINER (75866-307-01) |
| Product NDC | 75866-307 |
| 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, Inc. |
| Substance Name | OCTINOXATE; OXYBENZONE |
| Strength Number | 7; 3 |
| Strength Unit | g/100g; g/100g |
| Pharmaceutical Classes |
