NDC 76271-004

DR WALTONS VAPOR RUB

Vapor Rub

DR WALTONS VAPOR RUB is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Dr. Waltons, Incorporated. The primary component is Camphor (synthetic); Menthol; Eucalyptus Oil.

• Product ID: 76271-004_84149f61-14f9-44af-b3c3-6dec83130e07
• NDC: 76271-004
• Product Type: Human Otc Drug
• Proprietary Name: DR WALTONS VAPOR RUB
• Generic Name: Vapor Rub
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2011-07-14
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part346
• Labeler Name: DR. WALTONS, INCORPORATED
• Substance Name: CAMPHOR (SYNTHETIC); MENTHOL; EUCALYPTUS OIL
• Active Ingredient Strength: 5 g/113g; g/113g; g/113g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 76271-004-04

113 g in 1 JAR (76271-004-04)

• Marketing Start Date: 2011-07-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 76271-004-04 [76271000404]

DR WALTONS VAPOR RUB GEL

• Marketing Category: OTC monograph final
• Application Number: part346
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2011-07-14
• Inactivation Date: 2019-11-13

Drug Details

Active Ingredients

Ingredient	Strength
CAMPHOR (SYNTHETIC)	5.3 g/113g

OpenFDA Data

• SPL SET ID: 21cdd2e0-fefe-4d33-b79e-4687a2e3c5ab
• Manufacturer:
  • DR. WALTONS, INCORPORATED
• UNII:
  • 5TJD82A1ET
  • L7T10EIP3A
  • 2R04ONI662
• UPC Code:
  • 0850894003034

NDC Crossover Matching brand name "DR WALTONS VAPOR RUB" or generic name "Vapor Rub"

NDC	Brand Name	Generic Name
76271-004	DR WALTONS VAPOR RUB	VAPOR RUB
76176-018	PHARMACYS PRESCRIPTION	VAPOR RUB
69728-0020	VAPOUR RUB	VAPOR RUB
69728-0030	VAPOUR RUB	VAPOR RUB