NDC | 67777-005-00, 67777-005-10, 67777-005-50, 67777-005-70 |
Set ID | 81f5092d-0632-bf47-e053-2991aa0ac563 |
Category | HUMAN OTC DRUG LABEL |
Packager | Dynarex Corporation |
Generic Name | |
Product Class | |
Product Number | |
Application Number | PART347 |
- Active Ingredient
- Purpose
- Uses
- Warnings
- Directions
- Other Information
- 1140 Label
- 1141 Label
- 1145 Label
- 1147 Label
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INGREDIENTS AND APPEARANCE
WHITE PETROLATUM
petrolatum ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67777-005 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 1 g in 1 g Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67777-005-00 864 in 1 CASE 10/26/2018 1 144 in 1 BOX 1 5 g in 1 PACKET; Type 0: Not a Combination Product 2 NDC:67777-005-10 72 in 1 CASE 10/26/2018 2 1 in 1 BOX 2 28.4 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:67777-005-50 72 in 1 CASE 10/26/2018 3 6 in 1 BOX 3 113 g in 1 TUBE; Type 0: Not a Combination Product 4 NDC:67777-005-70 12 in 1 CASE 10/26/2018 4 425 g in 1 JAR; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/26/2018 Labeler - Dynarex Corporation (008124539)