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Advanced Relief A and D
Advanced Relief A and D - 42213-375-47 - (Petrolatum)
Drug Information of Advanced Relief A and D
| Product NDC: | 42213-375 |
| Proprietary Name: | Advanced Relief A and D |
| Non Proprietary Name: | Petrolatum |
| Active Ingredient(s): | 937.5 mg/g & nbsp; Petrolatum |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Advanced Relief A and D
| Product NDC: | 42213-375 |
| Labeler Name: | Ultra Seal Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part347 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111201 |
Package Information of Advanced Relief A and D
| Package NDC: | 42213-375-47 |
| Package Description: | 144 PACKET in 1 CARTON (42213-375-47) > 5 g in 1 PACKET (42213-375-05) |
NDC Information of Advanced Relief A and D
| NDC Code | 42213-375-47 |
| Proprietary Name | Advanced Relief A and D |
| Package Description | 144 PACKET in 1 CARTON (42213-375-47) > 5 g in 1 PACKET (42213-375-05) |
| Product NDC | 42213-375 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Petrolatum |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20111201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Ultra Seal Corporation |
| Substance Name | PETROLATUM |
| Strength Number | 937.5 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
