Label: AD PREVENT ORIGINAL ointment
- NDC Code(s): 65197-401-00, 65197-401-01, 65197-401-12
- Packager: WellSpring Pharmaceutical Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated February 1, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions?
- Distributed by:
-
PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
A+D PREVENT
Trusted for over 80 years
A+D® provides gentle and effective solutions for baby's precious skin.
A+D PREVENT
Original Ointment Diaper Rash Ointment + Skin Protectant
Helps prevent & treat diaper rash
Instantly forms a protective barrier to help seal out wetness
PEDIATRICIAN RECOMMENDED
PARABEN-FREE
DYE-FREE
PHTHALATE-FREE
NET WT 4OZ (113g)
NET WT 1.5OZ (42.5g)
A & D ORIGINAL OINTMENT 4oz
A & D ORIGINAL OINTMENT 1.5oz
A & D ORIGINAL OINTMENT 16oz
-
INGREDIENTS AND APPEARANCE
AD PREVENT ORIGINAL
ad prevent original ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:65197-401 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 15.5 g in 100 g PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM 53.4 g in 100 g Inactive Ingredients Ingredient Name Strength COD LIVER OIL (UNII: BBL281NWFG) LIGHT MINERAL OIL (UNII: N6K5787QVP) MICROCRYSTALLINE WAX (UNII: XOF597Q3KY) PARAFFIN (UNII: I9O0E3H2ZE) Product Characteristics Color orange (orange (Unctuous amber mass)) Score Shape Size Flavor Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:65197-401-01 1 in 1 BOX 10/02/2023 1 113 g in 1 TUBE; Type 0: Not a Combination Product 2 NDC:65197-401-12 1 in 1 BOX 10/02/2023 2 42.5 g in 1 TUBE; Type 0: Not a Combination Product 3 NDC:65197-401-00 454 g in 1 JAR; Type 0: Not a Combination Product 11/01/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M016 10/02/2023 Labeler - WellSpring Pharmaceutical Corporation (110999054)