NDC | 52810-103-12, 52810-103-13, 52810-103-52, 52810-103-53 |
Set ID | 3e8dfa74-8e63-41e4-a4d3-c6cfa805b215 |
Category | HUMAN OTC DRUG LABEL |
Packager | PUREMEDY |
Generic Name | |
Product Class | |
Product Number | |
Application Number |
- ACTIVE INGREDIENTS
- PURPOSE
-
USES
TEMPORARILY RELIEVES SYMPTOMS SUCH AS RED SPOTS, PUSTULES, BURNING AND OTHER IRRITATIONS ASSOCIATED WITH ACNE. PRODUCT USES ARE BASED ON HOMEOPATHIC MATERIA MEDICA. THESE 'USES' HAVE NOT BEEN EVALUATED BY THE FOOD AND DRUG ADMINISTRATION. THIS PRODUCT HAS NOT YET BEEN CLINICALLY TESTED BY PUREMEDY INC.
- DIRECTIONS
- INACTIVE INGREDIENTS
- WARNINGS
- KEEP OUT OF REACH OF CHILDREN.
- QUESTIONS OR COMMENTS?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
EXTRA DRAWING ACNE RELIEF
mahonia aquifolium, calendula officinalis, echinacea angustifolia, sambucus nigra, thuja occidentalis salveProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52810-103 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MAHONIA AQUIFOLIUM FRUITING TOP (UNII: P119855ERN) (MAHONIA AQUIFOLIUM FRUITING TOP - UNII:P119855ERN) MAHONIA AQUIFOLIUM FRUITING TOP 1 [hp_X] in 100 g CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD) (CALENDULA OFFICINALIS FLOWER - UNII:P0M7O4Y7YD) CALENDULA OFFICINALIS FLOWER 1 [hp_X] in 100 g ECHINACEA ANGUSTIFOLIA (UNII: VB06AV5US8) (ECHINACEA ANGUSTIFOLIA - UNII:VB06AV5US8) ECHINACEA ANGUSTIFOLIA 1 [hp_X] in 100 g SAMBUCUS NIGRA FLOWER (UNII: 07V4DX094T) (SAMBUCUS NIGRA FLOWER - UNII:07V4DX094T) SAMBUCUS NIGRA FLOWER 1 [hp_X] in 100 g THUJA OCCIDENTALIS LEAF (UNII: 0T0DQN8786) (THUJA OCCIDENTALIS LEAF - UNII:0T0DQN8786) THUJA OCCIDENTALIS LEAF 1 [hp_X] in 100 g Inactive Ingredients Ingredient Name Strength YELLOW WAX (UNII: 2ZA36H0S2V) SANGUINARIA CANADENSIS ROOT (UNII: N9288CD508) CANADA BALSAM (UNII: K304VI98I3) LAVENDER OIL (UNII: ZBP1YXW0H8) OLIVE OIL (UNII: 6UYK2W1W1E) PINUS MUGO SUBSP. MUGO LEAFY TWIG (UNII: 787BZ3D14H) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52810-103-12 28 g in 1 JAR; Type 0: Not a Combination Product 06/13/2016 2 NDC:52810-103-13 56 g in 1 JAR; Type 0: Not a Combination Product 06/13/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 06/13/2016 Labeler - PUREMEDY (003552251)