DR. RECKEWEG R17 COBRALACTIN COMBINATION PRODUCT- lacticum acidum 4x, naja tripudians 8x, scrophularia nodosa 2x liquid

DR. RECKEWEG R17 Cobralactin by

Drug Labeling and Warnings

DR. RECKEWEG R17 Cobralactin by is a Homeopathic medication manufactured, distributed, or labeled by PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredients

Lacticum acidum 4X, Naja tripudians 8X, Scrophularia nodosa 2X, 1 g each in 10 g.

PURPOSE

Purpose

Relieves of warts, growths, eczema, rashes

INDICATIONS & USAGE

Uses

For the temporary relief of:

• Warts
• Growths
• Eczem
• Rashes

WARNINGS

Warnings

Ask a doctor before use

• in children younger than 12 years.

Stop use and ask a doctor if

• condition worsens
  
• symptoms persist for more than 7 days
• symptoms clear up and occur again within a few days.

If pregnant or breastfeeding, ask a health care professional before use.

Keep out of reach of children.

DOSAGE & ADMINISTRATION

Directions
Adults and children ≥ 12 years 10-15 drops 3 times daily in a little water or undiluted or as recommended.

Not recommended for children under 12 years of age except under the advice of a health care professional.

OTHER SAFETY INFORMATION

Other information

• Tamper resistant: do not use if safety ring at base of cap is broken.
• Retain outer carton for full product information.

INACTIVE INGREDIENT

Inactive ingredients
Ethanol, purified water.

QUESTIONS

Questions?
Call 1-800-361-7872 or email questions@reckeweg.com

PRINCIPAL DISPLAY PANEL

NDC# 53346-1317-5

Dr. Reckeweg R17 Cobralactin

Homeopathic preparation for the temporary relief of:

• Warts
• Growths
• Eczema
• Rashes
  

Manufactured by:

Dr. Reckeweg Co. GmbH

D-64625 Bensheim

Germany

1.68 fl oz
(50 ml)

INGREDIENTS AND APPEARANCE

DR. RECKEWEG R17 COBRALACTIN  COMBINATION PRODUCT
lacticum acidum 4x, naja tripudians 8x, scrophularia nodosa 2x liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53346-1317
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LACTIC ACID, DL- (UNII: 3B8D35Y7S4) (LACTIC ACID, DL- - UNII:3B8D35Y7S4)	LACTIC ACID, DL-	4 [hp_X]  in 50 mL
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	8 [hp_X]  in 50 mL
SCROPHULARIA NODOSA (UNII: 7H443NUB2T) (SCROPHULARIA NODOSA - UNII:7H443NUB2T)	SCROPHULARIA NODOSA	2 [hp_X]  in 50 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53346-1317-5	50 mL in 1 BOTTLE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		06/01/1986

Labeler - PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO (318602612)

Establishment
Name	Address	ID/FEI	Business Operations
PHARMAZEUTISCHE FABRIK DR. RECKEWEG & CO		318602612	manufacture(53346-1317)