Label: LANA1263- lanolin ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 61767-232-01, 61767-232-02, 61767-232-03, 61767-232-04, view more61767-232-05, 61767-232-06 - 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
- Keep Out Of Reach Of Children
- Indications & Usage
- Dosage & Administration
- Other information:
- Inactive Ingredients
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
LANA1263
lanolin ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:61767-232 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H) LANOLIN 50 g in 100 g Inactive Ingredients Ingredient Name Strength WHITE WAX (UNII: 7G1J5DA97F) LANOLIN ALCOHOLS (UNII: 884C3FA9HE) MINERAL OIL (UNII: T5L8T28FGP) SODIUM BORATE (UNII: 91MBZ8H3QO) WATER (UNII: 059QF0KO0R) EDETIC ACID (UNII: 9G34HU7RV0) PETROLATUM (UNII: 4T6H12BN9U) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:61767-232-01 5 g in 1 PACKET 2 NDC:61767-232-02 15 g in 1 PACKET 3 NDC:61767-232-03 71 g in 1 JAR 4 NDC:61767-232-04 113 g in 1 TUBE 5 NDC:61767-232-05 127.5 g in 1 JAR 6 NDC:61767-232-06 396.8 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)