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NDC 49035-0922-01 Childrens Nighttime Cold and Mucus 6; 3; 6; 12; 6; 6; 3; 6; 30; 6; 12; 6; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details
Childrens Nighttime Cold and Mucus 6; 3; 6; 12; 6; 6; 3; 6; 30; 6; 12; 6; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
Childrens Nighttime Cold and Mucus is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores, Inc. The primary component is ANEMONE PULSATILLA; ARABICA COFFEE BEAN; BRYONIA ALBA ROOT; CALCIUM SULFIDE; EUPHRASIA STRICTA; GOLDENSEAL; MATRICARIA CHAMOMILLA; ONION; PHOSPHORUS; RUMEX CRISPUS ROOT; SILICON DIOXIDE; SODIUM CHLORIDE; SULFUR.
Product Information
| NDC | 49035-0922 |
|---|---|
| Product ID | 49035-922_d3b12415-abe4-2b99-e053-2995a90a991f |
| Associated GPIs | |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Childrens Nighttime Cold and Mucus |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | onion, bryonia alba root, arabica coffee bean, rumex crispus root, goldenseal, anemone pulsatilla, calcium sulfide, sulfur, phosphorus, matricaria chamomilla, euphrasia stricta, sodium chloride and silicon dioxide |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | LIQUID |
| Route | ORAL |
| Active Ingredient Strength | 6; 3; 6; 12; 6; 6; 3; 6; 30; 6; 12; 6; 12 |
| Active Ingredient Units | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Substance Name | ANEMONE PULSATILLA; ARABICA COFFEE BEAN; BRYONIA ALBA ROOT; CALCIUM SULFIDE; EUPHRASIA STRICTA; GOLDENSEAL; MATRICARIA CHAMOMILLA; ONION; PHOSPHORUS; RUMEX CRISPUS ROOT; SILICON DIOXIDE; SODIUM CHLORIDE; SULFUR |
| Labeler Name | Wal-Mart Stores, Inc |
| Pharmaceutical Class | Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED HOMEOPATHIC |
| Application Number | n/a |
| Listing Certified Through | 2022-12-31 |
Package
NDC 49035-0922-01 (49035092201)
| NDC Package Code | 49035-922-01 |
|---|---|
| Billing NDC | 49035092201 |
| Package | 118 mL in 1 BOTTLE, PLASTIC (49035-922-01) |
| Marketing Start Date | 2018-07-02 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |