Label: BRILLIA HEALTH COLD-FLU RECOVERY (lapine histamine immune globulin (12c, 30c, 50c), lapine interferon gamma immune globulin (12c, 30c, 50c), lapine cd4 immune globulin- 12c, 30c, 50c tablet
- NDC Code(s): 72123-006-01
- Packager: Hadaf LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated January 18, 2022
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- Official Label (Printer Friendly)
- Active Ingredients
- Purpose
- Uses
-
Warnings
Ask a doctor or pharmacist before use if you are lactose-intolerant.
Stop use and ask a doctor if symptoms persist or worsen.
If pregnant or breast-feeding, ask a health professional before use.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.
A llergic (hypersensitivity) reactions may occur in very rare cases.
Do not use if known sensitivity to Brillia Health Cold-Flu Recovery or any of its ingredients exists. - Ask a doctor
- STOP USE
- PREGNANCY OR BREAST FEEDING
- KEEP OUT OF REACH OF CHILDREN
- Allergic Reaction
- DO NOT USE
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Directions
• For adults and children 1 year and older.
• Hold tablet in mouth until completely dissolved, without food. If necessary, tablet can be taken dissolved in 1 tablespoon of drinking water.
• Day 1: 8 tablets total for the first day
1 tablet every 30 minutes for the first 2 hours
(a total of 5 tablets over 2 hours),
1 tablet taken 3 more times at equal intervals
(a total of 3 tablets over the remainder of the day).
• Days 2 to 5: 1 tablet 3 times a day
(at equal intervals). - Other Information
- Inactive Ingredients
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
BRILLIA HEALTH COLD-FLU RECOVERY
lapine histamine immune globulin (12c, 30c, 50c), lapine interferon gamma immune globulin (12c, 30c, 50c), lapine cd4 immune globulin (12c, 30c, 50c) tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72123-006 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LAPINE INTERFERON GAMMA IMMUNE GLOBULIN (UNII: Q2KS2OI6SA) (LAPINE INTERFERON GAMMA IMMUNE GLOBULIN - UNII:Q2KS2OI6SA) LAPINE INTERFERON GAMMA IMMUNE GLOBULIN 12 [hp_C] LAPINE HISTAMINE IMMUNE GLOBULIN (UNII: 7U4T47R0DD) (LAPINE HISTAMINE IMMUNE GLOBULIN - UNII:7U4T47R0DD) LAPINE HISTAMINE IMMUNE GLOBULIN 12 [hp_C] LAPINE CD4 IMMUNE GLOBULIN (UNII: UIF41K6WR9) (LAPINE CD4 IMMUNE GLOBULIN - UNII:UIF41K6WR9) LAPINE CD4 IMMUNE GLOBULIN 12 [hp_C] Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white Score score with uneven pieces Shape ROUND (round tablets) Size 9mm Flavor Imprint Code other Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72123-006-01 2 in 1 BOX 07/31/2020 1 20 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 07/31/2020 Labeler - Hadaf LLC (094114708) Establishment Name Address ID/FEI Business Operations Santonika Uab 520214047 manufacture(72123-006)