Label: DYNA1195- zinc oxide ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61767-226-01, 61767-226-02, 61767-226-03, 61767-226-04 - Packager: Blossom Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated October 23, 2014
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- ACTIVE INGREDIENT
- Purpose:
- Warnings:
- When using this product:
- Stop use and ask a doctor if:
- Keep out of reach of children.
- Dosage and Administration:
- Other information:
- INDICATIONS & USAGE
- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
DYNA1195
zinc oxide ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61767-226 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE 1.8 g in 100 g Inactive Ingredients Ingredient Name Strength LANOLIN (UNII: 7EV65EAW6H) CETETH-20 (UNII: I835H2IHHX) MINERAL OIL (UNII: T5L8T28FGP) METHYLPARABEN (UNII: A2I8C7HI9T) PROPYLPARABEN (UNII: Z8IX2SC1OH) GLYCERIN (UNII: PDC6A3C0OX) CETYL ALCOHOL (UNII: 936JST6JCN) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) CHOLECALCIFEROL (UNII: 1C6V77QF41) VITAMIN A (UNII: 81G40H8B0T) ALPHA-TOCOPHEROL (UNII: H4N855PNZ1) ALOE VERA LEAF (UNII: ZY81Z83H0X) PETROLATUM (UNII: 4T6H12BN9U) TROLAMINE (UNII: 9O3K93S3TK) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61767-226-01 5 g in 1 PACKET 2 NDC:61767-226-02 15 g in 1 PACKET 3 NDC:61767-226-03 114 g in 1 TUBE 4 NDC:61767-226-04 427.5 g in 1 JAR Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part347 10/23/2014 Labeler - Blossom Pharmaceuticals (677381470)