NDC 30775-051

Helix

Pain Relieving Cream

Helix is a Topical Cream in the Human Otc Drug category. It is labeled and distributed by Parker Laboratories, Inc.. The primary component is Menthol, Unspecified Form.

• Product ID: 30775-051_81a0e056-5f1a-7886-e053-2991aa0a4e29
• NDC: 30775-051
• Product Type: Human Otc Drug
• Proprietary Name: Helix
• Generic Name: Pain Relieving Cream
• Dosage Form: Cream
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-08-23
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Parker Laboratories, Inc.
• Substance Name: MENTHOL, UNSPECIFIED FORM
• Active Ingredient Strength: 7 g/100g
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 30775-051-01

4 BOX in 1 CASE (30775-051-01) > 100 PACKET in 1 BOX > 5 g in 1 PACKET

• Marketing Start Date: 2018-08-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 30775-051-32 [30775005132]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

NDC 30775-051-04 [30775005104]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

NDC 30775-051-50 [30775005150]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

NDC 30775-051-01 [30775005101]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

NDC 30775-051-12 [30775005112]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

NDC 30775-051-03 [30775005103]

Helix CREAM

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-08-23

Drug Details

Active Ingredients

Ingredient	Strength
MENTHOL, UNSPECIFIED FORM	7.4 g/100g

OpenFDA Data

• SPL SET ID: 73557911-4005-6e66-e053-2a91aa0ac620
• Manufacturer:
  • Parker Laboratories, Inc.
• UNII:
  • L7T10EIP3A
• RxNorm Concept Unique ID - RxCUI:
  • 2120690

NDC Crossover Matching brand name "Helix" or generic name "Pain Relieving Cream"

NDC	Brand Name	Generic Name
30775-051	Helix	Pain Relieving Cream
30775-053	Helix	CBD Therapy Cream
70338-621	BurnZone	Pain Relieving Cream
67777-113	DynaRub	Pain Relieving Cream
30775-052	Helix Tri-Active Therapy Cream	Pain Relieving Cream
50066-057	RAY DOL	Pain Relieving Cream