Itch Relief

Product NDC: 53799-220
11-digit product format: 537990220
Labeler code: 53799
Product ID: 53799-220_d4452115-6c33-4fc5-a362-f0f64ee8f13f
Type: HUMAN OTC DRUG
Nonproprietary name: apis mellifera, lachesis muta venom, ledum palustre twig and urtica urens
Dosage form: LIQUID
Route: TOPICAL
Labeler: Similasan AG
Marketing category: UNAPPROVED HOMEOPATHIC
Marketing start: 2021-04-23
Marketing end: 0000-00-00
Substance: APIS MELLIFERA; LACHESIS MUTA VENOM; LEDUM PALUSTRE TWIG; URTICA URENS
Active strength: 12 [hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL; [hp_X]/7.5mL
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
53799-220-42	2023-01-30	C162847	48780-1	f386c64a-0469-0266-e053-dadaa90a7c1a	Itch Relief

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
53799-220-42	Itch Relief	7.5 mL in 1 BOTTLE, WITH APPLICATOR	LIQUID	7.5		2
53799-220-42	Itch Relief	1 in 1 BOX	LIQUID	1		2

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
53799-220	ITCH RELIEF (APIS MELLIFERA, LACHESIS MUTA VENOM, LEDUM PALUSTRE TWIG AND URTICA URENS) LIQUID [SIMILASAN AG]	2	Legacy NDC, 2 package rows	20210424_9c0ab676-c8a4-4896-b91d-720d280a135d.zip

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
53799-220-42	53799022042	1 BOTTLE, WITH APPLICATOR in 1 BOX (53799-220-42) > 7.5 mL in 1 BOTTLE, WITH APPLICATOR	2021-04-23	0000-00-00	No	No	Current