NDC 59672-0732

TRIP EASE

Sodium Borate, Anamirta Cocculus Seed, Gelsemium Sempervirens Root, Wood Creosote, Toxicodendron Pubescens Leaf, And Tobacco Leaf

TRIP EASE is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Lc Industries. The primary component is Sodium Borate; Anamirta Cocculus Seed; Gelsemium Sempervirens Root; Wood Creosote; Toxicodendron Pubescens Leaf; Tobacco Leaf.

• Product ID: 59672-0732_977f1de9-3567-4053-ac35-eeb15012f936
• NDC: 59672-0732
• Product Type: Human Otc Drug
• Proprietary Name: TRIP EASE
• Generic Name: Sodium Borate, Anamirta Cocculus Seed, Gelsemium Sempervirens Root, Wood Creosote, Toxicodendron Pubescens Leaf, And Tobacco Leaf
• Dosage Form: Tablet
• Route of Administration: ORAL
• Marketing Start Date: 2012-05-04
• Marketing Category: UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC
• Labeler Name: LC Industries
• Substance Name: SODIUM BORATE; ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; WOOD CREOSOTE; TOXICODENDRON PUBESCENS LEAF; TOBACCO LEAF
• Active Ingredient Strength: 30 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 59672-0732-2

32 TABLET in 1 BLISTER PACK (59672-0732-2)

• Marketing Start Date: 2012-05-04
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 59672-0732-2 [59672073202]

TRIP EASE TABLET

• Marketing Category: UNAPPROVED HOMEOPATHIC
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-05-04
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
SODIUM BORATE	30 [hp_C]/1

OpenFDA Data

• SPL SET ID: 0034b407-fd1d-4e69-a468-83fe4e3c5aad
• Manufacturer:
  • LC Industries
• UNII:
  • 91MBZ8H3QO
  • 6IO182RP7A
  • 639KR60Q1Q
  • 810258W28U
  • 3JYG22FD73
  • 6YR2608RSU