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No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15
No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15 - 51630-004-01 - (Avobenzone, Octinoxate, Octocrylene)
Drug Information of No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15
| Product NDC: | 51630-004 |
| Proprietary Name: | No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15 |
| Non Proprietary Name: | Avobenzone, Octinoxate, Octocrylene |
| Active Ingredient(s): | 1.5; 2.5; .5 g/50g; g/50g; g/50g & nbsp; Avobenzone, Octinoxate, Octocrylene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15
| Product NDC: | 51630-004 |
| Labeler Name: | Schmid and Son Packaging |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part352 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20130122 |
Package Information of No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15
| Package NDC: | 51630-004-01 |
| Package Description: | 1 JAR in 1 CARTON (51630-004-01) > 50 g in 1 JAR |
NDC Information of No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15
| NDC Code | 51630-004-01 |
| Proprietary Name | No7 Lift and Luminate Day Sunscreen Broad Spectrum SPF 15 |
| Package Description | 1 JAR in 1 CARTON (51630-004-01) > 50 g in 1 JAR |
| Product NDC | 51630-004 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Avobenzone, Octinoxate, Octocrylene |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130122 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Schmid and Son Packaging |
| Substance Name | AVOBENZONE; OCTINOXATE; OCTOCRYLENE |
| Strength Number | 1.5; 2.5; .5 |
| Strength Unit | g/50g; g/50g; g/50g |
| Pharmaceutical Classes |
